Canonical Allele Identifier: CA399312922

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143291421
• MyVariant Identifiers: chr17:g.37883991G>T (hg19) ; chr17:g.39727738G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727738G>T , CM000679.2:g.39727738G>T	GRCh38
NC_000017.10:g.37883991G>T , CM000679.1:g.37883991G>T	GRCh37
NC_000017.9:g.35137517G>T	NCBI36
NG_007503.1:g.44599G>T , LRG_724:g.44599G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3462G>T MANE Select	ENSP00000269571.4:p.Glu1154Asp
ENST00000269571.9:c.3462G>T	ENSP00000269571.4:p.Glu1154Asp
ENST00000406381.6:c.3372G>T	ENSP00000385185.2:p.Glu1124Asp
ENST00000445658.6:c.2634G>T	ENSP00000404047.2:p.Glu878Asp
ENST00000541774.5:c.3417G>T	ENSP00000446466.1:p.Glu1139Asp
ENST00000578373.5:c.*3252G>T	ENSP00000463427.1:n.*3252G>T
ENST00000584450.5:c.*41G>T	ENSP00000463714.1:n.*41G>T
ENST00000584601.5:c.3372G>T	ENSP00000462438.1:p.Glu1124Asp
NM_001005862.2:c.3372G>T , LRG_724t1:c.3372G>T	NP_001005862.1:p.Glu1124Asp
NM_001289936.1:c.3417G>T , LRG_724t4:c.3417G>T	NP_001276865.1:p.Glu1139Asp
NM_001289937.1:c.*41G>T	NP_001276866.1:n.*41G>T
NM_004448.3:c.3462G>T , LRG_724t2:c.3462G>T	NP_004439.2:p.Glu1154Asp
NR_110535.1:n.3786G>T
XM_024450641.1:c.3600G>T	XP_024306409.1:p.Glu1200Asp
XM_024450642.1:c.3555G>T	XP_024306410.1:p.Glu1185Asp
XM_024450643.1:c.3510G>T	XP_024306411.1:p.Glu1170Asp
NM_001005862.3:c.3372G>T	NP_001005862.1:p.Glu1124Asp
NM_001289936.2:c.3417G>T	NP_001276865.1:p.Glu1139Asp
NM_001289937.2:c.*41G>T	NP_001276866.1:n.*41G>T
NM_001382782.1:c.3372G>T	NP_001369711.1:p.Glu1124Asp
NM_001382783.1:c.3372G>T	NP_001369712.1:p.Glu1124Asp
NM_001382784.1:c.3579G>T	NP_001369713.1:p.Glu1193Asp
NM_001382785.1:c.3564G>T	NP_001369714.1:p.Glu1188Asp
NM_001382786.1:c.3543G>T	NP_001369715.1:p.Glu1181Asp
NM_001382787.1:c.3537G>T	NP_001369716.1:p.Glu1179Asp
NM_001382788.1:c.3492G>T	NP_001369717.1:p.Glu1164Asp
NM_001382789.1:c.3483G>T	NP_001369718.1:p.Glu1161Asp
NM_001382790.1:c.3459G>T	NP_001369719.1:p.Glu1153Asp
NM_001382791.1:c.3453G>T	NP_001369720.1:p.Glu1151Asp
NM_001382792.1:c.3426G>T	NP_001369721.1:p.Glu1142Asp
NM_001382793.1:c.3420G>T	NP_001369722.1:p.Glu1140Asp
NM_001382794.1:c.3420G>T	NP_001369723.1:p.Glu1140Asp
NM_001382795.1:c.3414G>T	NP_001369724.1:p.Glu1138Asp
NM_001382796.1:c.3375G>T	NP_001369725.1:p.Glu1125Asp
NM_001382797.1:c.3363G>T	NP_001369726.1:p.Glu1121Asp
NM_001382798.1:c.3306G>T	NP_001369727.1:p.Glu1102Asp
NM_001382799.1:c.3282G>T	NP_001369728.1:p.Glu1094Asp
NM_001382800.1:c.3276G>T	NP_001369729.1:p.Glu1092Asp
NM_001382801.1:c.3258G>T	NP_001369730.1:p.Glu1086Asp
NM_001382802.1:c.3204G>T	NP_001369731.1:p.Glu1068Asp
NM_001382803.1:c.*41G>T	NP_001369732.1:n.*41G>T
NM_001382804.1:c.2634G>T	NP_001369733.1:p.Glu878Asp
NM_001382805.1:c.2511G>T	NP_001369734.1:p.Glu837Asp
NM_001382806.1:c.2424G>T	NP_001369735.1:p.Glu808Asp
NM_004448.4:c.3462G>T MANE Select	NP_004439.2:p.Glu1154Asp
NR_110535.2:n.3700G>T