Canonical Allele Identifier: CA399313444

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143300349
• MyVariant Identifiers: chr17:g.37884071T>A (hg19) ; chr17:g.39727818T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727818T>A , CM000679.2:g.39727818T>A	GRCh38
NC_000017.10:g.37884071T>A , CM000679.1:g.37884071T>A	GRCh37
NC_000017.9:g.35137597T>A	NCBI36
NG_007503.1:g.44679T>A , LRG_724:g.44679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3542T>A MANE Select	ENSP00000269571.4:p.Val1181Asp
ENST00000269571.9:c.3542T>A	ENSP00000269571.4:p.Val1181Asp
ENST00000406381.6:c.3452T>A	ENSP00000385185.2:p.Val1151Asp
ENST00000445658.6:c.2714T>A	ENSP00000404047.2:p.Val905Asp
ENST00000541774.5:c.3497T>A	ENSP00000446466.1:p.Val1166Asp
ENST00000578373.5:c.*3332T>A	ENSP00000463427.1:n.*3332T>A
ENST00000584450.5:c.*121T>A	ENSP00000463714.1:n.*121T>A
ENST00000584601.5:c.3452T>A	ENSP00000462438.1:p.Val1151Asp
NM_001005862.2:c.3452T>A , LRG_724t1:c.3452T>A	NP_001005862.1:p.Val1151Asp
NM_001289936.1:c.3497T>A , LRG_724t4:c.3497T>A	NP_001276865.1:p.Val1166Asp
NM_001289937.1:c.*121T>A	NP_001276866.1:n.*121T>A
NM_004448.3:c.3542T>A , LRG_724t2:c.3542T>A	NP_004439.2:p.Val1181Asp
NR_110535.1:n.3866T>A
XM_024450641.1:c.3680T>A	XP_024306409.1:p.Val1227Asp
XM_024450642.1:c.3635T>A	XP_024306410.1:p.Val1212Asp
XM_024450643.1:c.3590T>A	XP_024306411.1:p.Val1197Asp
NM_001005862.3:c.3452T>A	NP_001005862.1:p.Val1151Asp
NM_001289936.2:c.3497T>A	NP_001276865.1:p.Val1166Asp
NM_001289937.2:c.*121T>A	NP_001276866.1:n.*121T>A
NM_001382782.1:c.3452T>A	NP_001369711.1:p.Val1151Asp
NM_001382783.1:c.3452T>A	NP_001369712.1:p.Val1151Asp
NM_001382784.1:c.3659T>A	NP_001369713.1:p.Val1220Asp
NM_001382785.1:c.3644T>A	NP_001369714.1:p.Val1215Asp
NM_001382786.1:c.3623T>A	NP_001369715.1:p.Val1208Asp
NM_001382787.1:c.3617T>A	NP_001369716.1:p.Val1206Asp
NM_001382788.1:c.3572T>A	NP_001369717.1:p.Val1191Asp
NM_001382789.1:c.3563T>A	NP_001369718.1:p.Val1188Asp
NM_001382790.1:c.3539T>A	NP_001369719.1:p.Val1180Asp
NM_001382791.1:c.3533T>A	NP_001369720.1:p.Val1178Asp
NM_001382792.1:c.3506T>A	NP_001369721.1:p.Val1169Asp
NM_001382793.1:c.3500T>A	NP_001369722.1:p.Val1167Asp
NM_001382794.1:c.3500T>A	NP_001369723.1:p.Val1167Asp
NM_001382795.1:c.3494T>A	NP_001369724.1:p.Val1165Asp
NM_001382796.1:c.3455T>A	NP_001369725.1:p.Val1152Asp
NM_001382797.1:c.3443T>A	NP_001369726.1:p.Val1148Asp
NM_001382798.1:c.3386T>A	NP_001369727.1:p.Val1129Asp
NM_001382799.1:c.3362T>A	NP_001369728.1:p.Val1121Asp
NM_001382800.1:c.3356T>A	NP_001369729.1:p.Val1119Asp
NM_001382801.1:c.3338T>A	NP_001369730.1:p.Val1113Asp
NM_001382802.1:c.3284T>A	NP_001369731.1:p.Val1095Asp
NM_001382803.1:c.*121T>A	NP_001369732.1:n.*121T>A
NM_001382804.1:c.2714T>A	NP_001369733.1:p.Val905Asp
NM_001382805.1:c.2591T>A	NP_001369734.1:p.Val864Asp
NM_001382806.1:c.2504T>A	NP_001369735.1:p.Val835Asp
NM_004448.4:c.3542T>A MANE Select	NP_004439.2:p.Val1181Asp
NR_110535.2:n.3780T>A