Canonical Allele Identifier: CA626209437
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs1292830249

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727804del , CM000679.2:g.39727804del GRCh38
NC_000017.10:g.37884057del , CM000679.1:g.37884057del GRCh37
NC_000017.9:g.35137583del NCBI36
NG_007503.1:g.44665del , LRG_724:g.44665del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3528del MANE Select ENSP00000269571.4:p.Lys1177ArgfsTer21
ENST00000269571.9:c.3528del ENSP00000269571.4:p.Lys1177ArgfsTer21
ENST00000406381.6:c.3438del ENSP00000385185.2:p.Lys1147ArgfsTer21
ENST00000445658.6:c.2700del ENSP00000404047.2:p.Lys901ArgfsTer21
ENST00000541774.5:c.3483del ENSP00000446466.1:p.Lys1162ArgfsTer21
ENST00000578373.5:c.*3318del ENSP00000463427.1:n.*3318del
ENST00000584450.5:c.*107del ENSP00000463714.1:n.*107del
ENST00000584601.5:c.3438del ENSP00000462438.1:p.Lys1147ArgfsTer21
NM_001005862.2:c.3438del , LRG_724t1:c.3438del NP_001005862.1:p.Lys1147ArgfsTer21
NM_001289936.1:c.3483del , LRG_724t4:c.3483del NP_001276865.1:p.Lys1162ArgfsTer21
NM_001289937.1:c.*107del NP_001276866.1:n.*107del
NM_004448.3:c.3528del , LRG_724t2:c.3528del NP_004439.2:p.Lys1177ArgfsTer21
NR_110535.1:n.3852del
XM_024450641.1:c.3666del XP_024306409.1:p.Lys1223ArgfsTer21
XM_024450642.1:c.3621del XP_024306410.1:p.Lys1208ArgfsTer21
XM_024450643.1:c.3576del XP_024306411.1:p.Lys1193ArgfsTer21
NM_001005862.3:c.3438del NP_001005862.1:p.Lys1147ArgfsTer21
NM_001289936.2:c.3483del NP_001276865.1:p.Lys1162ArgfsTer21
NM_001289937.2:c.*107del NP_001276866.1:n.*107del
NM_001382782.1:c.3438del NP_001369711.1:p.Lys1147ArgfsTer21
NM_001382783.1:c.3438del NP_001369712.1:p.Lys1147ArgfsTer21
NM_001382784.1:c.3645del NP_001369713.1:p.Lys1216ArgfsTer21
NM_001382785.1:c.3630del NP_001369714.1:p.Lys1211ArgfsTer21
NM_001382786.1:c.3609del NP_001369715.1:p.Lys1204ArgfsTer21
NM_001382787.1:c.3603del NP_001369716.1:p.Lys1202ArgfsTer21
NM_001382788.1:c.3558del NP_001369717.1:p.Lys1187ArgfsTer21
NM_001382789.1:c.3549del NP_001369718.1:p.Lys1184ArgfsTer21
NM_001382790.1:c.3525del NP_001369719.1:p.Lys1176ArgfsTer21
NM_001382791.1:c.3519del NP_001369720.1:p.Lys1174ArgfsTer21
NM_001382792.1:c.3492del NP_001369721.1:p.Lys1165ArgfsTer21
NM_001382793.1:c.3486del NP_001369722.1:p.Lys1163ArgfsTer21
NM_001382794.1:c.3486del NP_001369723.1:p.Lys1163ArgfsTer21
NM_001382795.1:c.3480del NP_001369724.1:p.Lys1161ArgfsTer21
NM_001382796.1:c.3441del NP_001369725.1:p.Lys1148ArgfsTer21
NM_001382797.1:c.3429del NP_001369726.1:p.Lys1144ArgfsTer21
NM_001382798.1:c.3372del NP_001369727.1:p.Lys1125ArgfsTer21
NM_001382799.1:c.3348del NP_001369728.1:p.Lys1117ArgfsTer21
NM_001382800.1:c.3342del NP_001369729.1:p.Lys1115ArgfsTer21
NM_001382801.1:c.3324del NP_001369730.1:p.Lys1109ArgfsTer21
NM_001382802.1:c.3270del NP_001369731.1:p.Lys1091ArgfsTer21
NM_001382803.1:c.*107del NP_001369732.1:n.*107del
NM_001382804.1:c.2700del NP_001369733.1:p.Lys901ArgfsTer21
NM_001382805.1:c.2577del NP_001369734.1:p.Lys860ArgfsTer21
NM_001382806.1:c.2490del NP_001369735.1:p.Lys831ArgfsTer21
NM_004448.4:c.3528del MANE Select NP_004439.2:p.Lys1177ArgfsTer21
NR_110535.2:n.3766del