Canonical Allele Identifier: CA983630520
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2059616116

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724276_39724277insCTTTTTTTTTTTTTTTTTTTTTT , CM000679.2:g.39724276_39724277insCTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000017.10:g.37880529_37880530insCTTTTTTTTTTTTTTTTTTTTTT , CM000679.1:g.37880529_37880530insCTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000017.9:g.35134055_35134056insCTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_007503.1:g.41137_41138insCTTTTTTTTTTTTTTTTTTTTTT , LRG_724:g.41137_41138insCTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000269571.4:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTT...
ENST00000269571.9:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT ENSP00000269571.4:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTT...
ENST00000406381.6:c.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT ENSP00000385185.2:n.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTT...
ENST00000445658.6:c.1479+266_1479+267insCTTTTTTTTTTTTTTTTTTTTTT ENSP00000404047.2:n.1479+266_1479+267insCTTTTTTTTTTTTTTTTTTTT...
ENST00000541774.5:c.2262+266_2262+267insCTTTTTTTTTTTTTTTTTTTTTT ENSP00000446466.1:n.2262+266_2262+267insCTTTTTTTTTTTTTTTTTTTT...
ENST00000578373.5:c.*2097+266_*2097+267insCTTTTTTTTTTTTTTTTTTTTTT ENSP00000463427.1:n.*2097+266_*2097+267insCTTTTTTTTTTTTTTTTTT...
ENST00000580074.1:c.413+266_413+267insCTTTTTTTTTTTTTTTTTTTTTT
ENST00000583038.5:n.3441+266_3441+267insCTTTTTTTTTTTTTTTTTTTTTT
ENST00000584450.5:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT ENSP00000463714.1:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTT...
ENST00000584601.5:c.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT ENSP00000462438.1:n.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTT...
NM_001005862.2:c.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT , LRG_724t1:c.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001005862.1:n.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001289936.1:c.2262+266_2262+267insCTTTTTTTTTTTTTTTTTTTTTT , LRG_724t4:c.2262+266_2262+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001276865.1:n.2262+266_2262+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001289937.1:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001276866.1:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_004448.3:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT , LRG_724t2:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT NP_004439.2:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT
NR_110535.1:n.2631+266_2631+267insCTTTTTTTTTTTTTTTTTTTTTT
XM_024450641.1:c.2445+266_2445+267insCTTTTTTTTTTTTTTTTTTTTTT XP_024306409.1:n.2445+266_2445+267insCTTTTTTTTTTTTTTTTTTTTTT
XM_024450642.1:c.2400+266_2400+267insCTTTTTTTTTTTTTTTTTTTTTT XP_024306410.1:n.2400+266_2400+267insCTTTTTTTTTTTTTTTTTTTTTT
XM_024450643.1:c.2355+266_2355+267insCTTTTTTTTTTTTTTTTTTTTTT XP_024306411.1:n.2355+266_2355+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001005862.3:c.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001005862.1:n.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001289936.2:c.2262+266_2262+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001276865.1:n.2262+266_2262+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001289937.2:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001276866.1:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382782.1:c.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369711.1:n.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382783.1:c.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369712.1:n.2217+266_2217+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382784.1:c.2424+266_2424+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369713.1:n.2424+266_2424+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382785.1:c.2409+266_2409+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369714.1:n.2409+266_2409+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382786.1:c.2388+266_2388+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369715.1:n.2388+266_2388+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382787.1:c.2382+266_2382+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369716.1:n.2382+266_2382+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382788.1:c.2337+266_2337+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369717.1:n.2337+266_2337+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382789.1:c.2328+266_2328+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369718.1:n.2328+266_2328+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382790.1:c.2304+266_2304+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369719.1:n.2304+266_2304+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382791.1:c.2298+266_2298+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369720.1:n.2298+266_2298+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382792.1:c.2271+266_2271+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369721.1:n.2271+266_2271+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382793.1:c.2265+266_2265+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369722.1:n.2265+266_2265+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382794.1:c.2265+266_2265+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369723.1:n.2265+266_2265+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382795.1:c.2259+266_2259+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369724.1:n.2259+266_2259+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382796.1:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369725.1:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382797.1:c.2209-450_2209-449insCTTTTTTTTTTTTTTTTTTTTTT NP_001369726.1:n.2209-450_2209-449insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382798.1:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369727.1:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382799.1:c.2127+266_2127+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369728.1:n.2127+266_2127+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382800.1:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369729.1:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382801.1:c.2259+266_2259+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369730.1:n.2259+266_2259+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382802.1:c.2049+266_2049+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369731.1:n.2049+266_2049+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382803.1:c.2265+266_2265+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369732.1:n.2265+266_2265+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382804.1:c.1479+266_1479+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369733.1:n.1479+266_1479+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382805.1:c.2208+616_2208+617insCTTTTTTTTTTTTTTTTTTTTTT NP_001369734.1:n.2208+616_2208+617insCTTTTTTTTTTTTTTTTTTTTTT
NM_001382806.1:c.1269+266_1269+267insCTTTTTTTTTTTTTTTTTTTTTT NP_001369735.1:n.1269+266_1269+267insCTTTTTTTTTTTTTTTTTTTTTT
NM_004448.4:c.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_004439.2:n.2307+266_2307+267insCTTTTTTTTTTTTTTTTTTTTTT
NR_110535.2:n.2545+266_2545+267insCTTTTTTTTTTTTTTTTTTTTTT