Canonical Allele Identifier: CA399310285

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143237051
• MyVariant Identifiers: chr17:g.37883597C>A (hg19) ; chr17:g.39727344C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727344C>A , CM000679.2:g.39727344C>A	GRCh38
NC_000017.10:g.37883597C>A , CM000679.1:g.37883597C>A	GRCh37
NC_000017.9:g.35137123C>A	NCBI36
NG_007503.1:g.44205C>A , LRG_724:g.44205C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3209C>A MANE Select	ENSP00000269571.4:p.Ala1070Asp
ENST00000269571.9:c.3209C>A	ENSP00000269571.4:p.Ala1070Asp
ENST00000406381.6:c.3119C>A	ENSP00000385185.2:p.Ala1040Asp
ENST00000445658.6:c.2381C>A	ENSP00000404047.2:p.Ala794Asp
ENST00000541774.5:c.3164C>A	ENSP00000446466.1:p.Ala1055Asp
ENST00000578373.5:c.*2999C>A	ENSP00000463427.1:n.*2999C>A
ENST00000584450.5:c.3159+341C>A	ENSP00000463714.1:n.3159+341C>A
ENST00000584601.5:c.3119C>A	ENSP00000462438.1:p.Ala1040Asp
NM_001005862.2:c.3119C>A , LRG_724t1:c.3119C>A	NP_001005862.1:p.Ala1040Asp
NM_001289936.1:c.3164C>A , LRG_724t4:c.3164C>A	NP_001276865.1:p.Ala1055Asp
NM_001289937.1:c.3159+341C>A	NP_001276866.1:n.3159+341C>A
NM_004448.3:c.3209C>A , LRG_724t2:c.3209C>A	NP_004439.2:p.Ala1070Asp
NR_110535.1:n.3533C>A
XM_024450641.1:c.3347C>A	XP_024306409.1:p.Ala1116Asp
XM_024450642.1:c.3302C>A	XP_024306410.1:p.Ala1101Asp
XM_024450643.1:c.3257C>A	XP_024306411.1:p.Ala1086Asp
NM_001005862.3:c.3119C>A	NP_001005862.1:p.Ala1040Asp
NM_001289936.2:c.3164C>A	NP_001276865.1:p.Ala1055Asp
NM_001289937.2:c.3159+341C>A	NP_001276866.1:n.3159+341C>A
NM_001382782.1:c.3119C>A	NP_001369711.1:p.Ala1040Asp
NM_001382783.1:c.3119C>A	NP_001369712.1:p.Ala1040Asp
NM_001382784.1:c.3326C>A	NP_001369713.1:p.Ala1109Asp
NM_001382785.1:c.3311C>A	NP_001369714.1:p.Ala1104Asp
NM_001382786.1:c.3290C>A	NP_001369715.1:p.Ala1097Asp
NM_001382787.1:c.3284C>A	NP_001369716.1:p.Ala1095Asp
NM_001382788.1:c.3239C>A	NP_001369717.1:p.Ala1080Asp
NM_001382789.1:c.3230C>A	NP_001369718.1:p.Ala1077Asp
NM_001382790.1:c.3206C>A	NP_001369719.1:p.Ala1069Asp
NM_001382791.1:c.3200C>A	NP_001369720.1:p.Ala1067Asp
NM_001382792.1:c.3173C>A	NP_001369721.1:p.Ala1058Asp
NM_001382793.1:c.3167C>A	NP_001369722.1:p.Ala1056Asp
NM_001382794.1:c.3167C>A	NP_001369723.1:p.Ala1056Asp
NM_001382795.1:c.3161C>A	NP_001369724.1:p.Ala1054Asp
NM_001382796.1:c.3122C>A	NP_001369725.1:p.Ala1041Asp
NM_001382797.1:c.3110C>A	NP_001369726.1:p.Ala1037Asp
NM_001382798.1:c.3053C>A	NP_001369727.1:p.Ala1018Asp
NM_001382799.1:c.3029C>A	NP_001369728.1:p.Ala1010Asp
NM_001382800.1:c.3023C>A	NP_001369729.1:p.Ala1008Asp
NM_001382801.1:c.3005C>A	NP_001369730.1:p.Ala1002Asp
NM_001382802.1:c.2951C>A	NP_001369731.1:p.Ala984Asp
NM_001382803.1:c.3117+341C>A	NP_001369732.1:n.3117+341C>A
NM_001382804.1:c.2381C>A	NP_001369733.1:p.Ala794Asp
NM_001382805.1:c.2258C>A	NP_001369734.1:p.Ala753Asp
NM_001382806.1:c.2171C>A	NP_001369735.1:p.Ala724Asp
NM_004448.4:c.3209C>A MANE Select	NP_004439.2:p.Ala1070Asp
NR_110535.2:n.3447C>A