Canonical Allele Identifier: CA919838675
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs1567912444

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724271_39724272insTTTTTTTTTTTTTTTTTTTTTT , CM000679.2:g.39724271_39724272insTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000017.10:g.37880524_37880525insTTTTTTTTTTTTTTTTTTTTTT , CM000679.1:g.37880524_37880525insTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000017.9:g.35134050_35134051insTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_007503.1:g.41132_41133insTTTTTTTTTTTTTTTTTTTTTT , LRG_724:g.41132_41133insTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000269571.4:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTT...
ENST00000269571.9:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT ENSP00000269571.4:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTT...
ENST00000406381.6:c.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT ENSP00000385185.2:n.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTT...
ENST00000445658.6:c.1479+261_1479+262insTTTTTTTTTTTTTTTTTTTTTT ENSP00000404047.2:n.1479+261_1479+262insTTTTTTTTTTTTTTTTTTTTT...
ENST00000541774.5:c.2262+261_2262+262insTTTTTTTTTTTTTTTTTTTTTT ENSP00000446466.1:n.2262+261_2262+262insTTTTTTTTTTTTTTTTTTTTT...
ENST00000578373.5:c.*2097+261_*2097+262insTTTTTTTTTTTTTTTTTTTTTT ENSP00000463427.1:n.*2097+261_*2097+262insTTTTTTTTTTTTTTTTTTT...
ENST00000580074.1:c.413+261_413+262insTTTTTTTTTTTTTTTTTTTTTT
ENST00000583038.5:n.3441+261_3441+262insTTTTTTTTTTTTTTTTTTTTTT
ENST00000584450.5:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT ENSP00000463714.1:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTT...
ENST00000584601.5:c.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT ENSP00000462438.1:n.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTT...
NM_001005862.2:c.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT , LRG_724t1:c.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT NP_001005862.1:n.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001289936.1:c.2262+261_2262+262insTTTTTTTTTTTTTTTTTTTTTT , LRG_724t4:c.2262+261_2262+262insTTTTTTTTTTTTTTTTTTTTTT NP_001276865.1:n.2262+261_2262+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001289937.1:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT NP_001276866.1:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT
NM_004448.3:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT , LRG_724t2:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT NP_004439.2:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT
NR_110535.1:n.2631+261_2631+262insTTTTTTTTTTTTTTTTTTTTTT
XM_024450641.1:c.2445+261_2445+262insTTTTTTTTTTTTTTTTTTTTTT XP_024306409.1:n.2445+261_2445+262insTTTTTTTTTTTTTTTTTTTTTT
XM_024450642.1:c.2400+261_2400+262insTTTTTTTTTTTTTTTTTTTTTT XP_024306410.1:n.2400+261_2400+262insTTTTTTTTTTTTTTTTTTTTTT
XM_024450643.1:c.2355+261_2355+262insTTTTTTTTTTTTTTTTTTTTTT XP_024306411.1:n.2355+261_2355+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001005862.3:c.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT NP_001005862.1:n.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001289936.2:c.2262+261_2262+262insTTTTTTTTTTTTTTTTTTTTTT NP_001276865.1:n.2262+261_2262+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001289937.2:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT NP_001276866.1:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382782.1:c.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369711.1:n.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382783.1:c.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369712.1:n.2217+261_2217+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382784.1:c.2424+261_2424+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369713.1:n.2424+261_2424+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382785.1:c.2409+261_2409+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369714.1:n.2409+261_2409+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382786.1:c.2388+261_2388+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369715.1:n.2388+261_2388+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382787.1:c.2382+261_2382+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369716.1:n.2382+261_2382+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382788.1:c.2337+261_2337+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369717.1:n.2337+261_2337+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382789.1:c.2328+261_2328+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369718.1:n.2328+261_2328+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382790.1:c.2304+261_2304+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369719.1:n.2304+261_2304+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382791.1:c.2298+261_2298+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369720.1:n.2298+261_2298+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382792.1:c.2271+261_2271+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369721.1:n.2271+261_2271+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382793.1:c.2265+261_2265+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369722.1:n.2265+261_2265+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382794.1:c.2265+261_2265+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369723.1:n.2265+261_2265+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382795.1:c.2259+261_2259+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369724.1:n.2259+261_2259+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382796.1:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369725.1:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382797.1:c.2209-455_2209-454insTTTTTTTTTTTTTTTTTTTTTT NP_001369726.1:n.2209-455_2209-454insTTTTTTTTTTTTTTTTTTTTTT
NM_001382798.1:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369727.1:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382799.1:c.2127+261_2127+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369728.1:n.2127+261_2127+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382800.1:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369729.1:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382801.1:c.2259+261_2259+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369730.1:n.2259+261_2259+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382802.1:c.2049+261_2049+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369731.1:n.2049+261_2049+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382803.1:c.2265+261_2265+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369732.1:n.2265+261_2265+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382804.1:c.1479+261_1479+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369733.1:n.1479+261_1479+262insTTTTTTTTTTTTTTTTTTTTTT
NM_001382805.1:c.2208+611_2208+612insTTTTTTTTTTTTTTTTTTTTTT NP_001369734.1:n.2208+611_2208+612insTTTTTTTTTTTTTTTTTTTTTT
NM_001382806.1:c.1269+261_1269+262insTTTTTTTTTTTTTTTTTTTTTT NP_001369735.1:n.1269+261_1269+262insTTTTTTTTTTTTTTTTTTTTTT
NM_004448.4:c.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_004439.2:n.2307+261_2307+262insTTTTTTTTTTTTTTTTTTTTTT
NR_110535.2:n.2545+261_2545+262insTTTTTTTTTTTTTTTTTTTTTT