Canonical Allele Identifier: CA625937572
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs1243809159

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724290_39724291insTTTTTTTTTTTTTTTTTTTTTTT , CM000679.2:g.39724290_39724291insTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000017.10:g.37880543_37880544insTTTTTTTTTTTTTTTTTTTTTTT , CM000679.1:g.37880543_37880544insTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000017.9:g.35134069_35134070insTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_007503.1:g.41151_41152insTTTTTTTTTTTTTTTTTTTTTTT , LRG_724:g.41151_41152insTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000269571.4:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTT...
ENST00000269571.9:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT ENSP00000269571.4:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTT...
ENST00000406381.6:c.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT ENSP00000385185.2:n.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTT...
ENST00000445658.6:c.1479+280_1479+281insTTTTTTTTTTTTTTTTTTTTTTT ENSP00000404047.2:n.1479+280_1479+281insTTTTTTTTTTTTTTTTTTTTT...
ENST00000541774.5:c.2262+280_2262+281insTTTTTTTTTTTTTTTTTTTTTTT ENSP00000446466.1:n.2262+280_2262+281insTTTTTTTTTTTTTTTTTTTTT...
ENST00000578373.5:c.*2097+280_*2097+281insTTTTTTTTTTTTTTTTTTTTTTT ENSP00000463427.1:n.*2097+280_*2097+281insTTTTTTTTTTTTTTTTTTT...
ENST00000580074.1:c.413+280_413+281insTTTTTTTTTTTTTTTTTTTTTTT
ENST00000583038.5:n.3441+280_3441+281insTTTTTTTTTTTTTTTTTTTTTTT
ENST00000584450.5:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT ENSP00000463714.1:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTT...
ENST00000584601.5:c.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT ENSP00000462438.1:n.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTT...
NM_001005862.2:c.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT , LRG_724t1:c.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001005862.1:n.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001289936.1:c.2262+280_2262+281insTTTTTTTTTTTTTTTTTTTTTTT , LRG_724t4:c.2262+280_2262+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001276865.1:n.2262+280_2262+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001289937.1:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001276866.1:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_004448.3:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT , LRG_724t2:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT NP_004439.2:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT
NR_110535.1:n.2631+280_2631+281insTTTTTTTTTTTTTTTTTTTTTTT
XM_024450641.1:c.2445+280_2445+281insTTTTTTTTTTTTTTTTTTTTTTT XP_024306409.1:n.2445+280_2445+281insTTTTTTTTTTTTTTTTTTTTTTT
XM_024450642.1:c.2400+280_2400+281insTTTTTTTTTTTTTTTTTTTTTTT XP_024306410.1:n.2400+280_2400+281insTTTTTTTTTTTTTTTTTTTTTTT
XM_024450643.1:c.2355+280_2355+281insTTTTTTTTTTTTTTTTTTTTTTT XP_024306411.1:n.2355+280_2355+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001005862.3:c.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001005862.1:n.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001289936.2:c.2262+280_2262+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001276865.1:n.2262+280_2262+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001289937.2:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001276866.1:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382782.1:c.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369711.1:n.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382783.1:c.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369712.1:n.2217+280_2217+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382784.1:c.2424+280_2424+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369713.1:n.2424+280_2424+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382785.1:c.2409+280_2409+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369714.1:n.2409+280_2409+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382786.1:c.2388+280_2388+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369715.1:n.2388+280_2388+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382787.1:c.2382+280_2382+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369716.1:n.2382+280_2382+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382788.1:c.2337+280_2337+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369717.1:n.2337+280_2337+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382789.1:c.2328+280_2328+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369718.1:n.2328+280_2328+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382790.1:c.2304+280_2304+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369719.1:n.2304+280_2304+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382791.1:c.2298+280_2298+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369720.1:n.2298+280_2298+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382792.1:c.2271+280_2271+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369721.1:n.2271+280_2271+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382793.1:c.2265+280_2265+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369722.1:n.2265+280_2265+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382794.1:c.2265+280_2265+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369723.1:n.2265+280_2265+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382795.1:c.2259+280_2259+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369724.1:n.2259+280_2259+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382796.1:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369725.1:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382797.1:c.2209-436_2209-435insTTTTTTTTTTTTTTTTTTTTTTT NP_001369726.1:n.2209-436_2209-435insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382798.1:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369727.1:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382799.1:c.2127+280_2127+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369728.1:n.2127+280_2127+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382800.1:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369729.1:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382801.1:c.2259+280_2259+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369730.1:n.2259+280_2259+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382802.1:c.2049+280_2049+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369731.1:n.2049+280_2049+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382803.1:c.2265+280_2265+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369732.1:n.2265+280_2265+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382804.1:c.1479+280_1479+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369733.1:n.1479+280_1479+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382805.1:c.2208+630_2208+631insTTTTTTTTTTTTTTTTTTTTTTT NP_001369734.1:n.2208+630_2208+631insTTTTTTTTTTTTTTTTTTTTTTT
NM_001382806.1:c.1269+280_1269+281insTTTTTTTTTTTTTTTTTTTTTTT NP_001369735.1:n.1269+280_1269+281insTTTTTTTTTTTTTTTTTTTTTTT
NM_004448.4:c.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_004439.2:n.2307+280_2307+281insTTTTTTTTTTTTTTTTTTTTTTT
NR_110535.2:n.2545+280_2545+281insTTTTTTTTTTTTTTTTTTTTTTT