Canonical Allele Identifier: CA399312917

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143291314
• MyVariant Identifiers: chr17:g.37883990A>T (hg19) ; chr17:g.39727737A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727737A>T , CM000679.2:g.39727737A>T	GRCh38
NC_000017.10:g.37883990A>T , CM000679.1:g.37883990A>T	GRCh37
NC_000017.9:g.35137516A>T	NCBI36
NG_007503.1:g.44598A>T , LRG_724:g.44598A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3461A>T MANE Select	ENSP00000269571.4:p.Glu1154Val
ENST00000269571.9:c.3461A>T	ENSP00000269571.4:p.Glu1154Val
ENST00000406381.6:c.3371A>T	ENSP00000385185.2:p.Glu1124Val
ENST00000445658.6:c.2633A>T	ENSP00000404047.2:p.Glu878Val
ENST00000541774.5:c.3416A>T	ENSP00000446466.1:p.Glu1139Val
ENST00000578373.5:c.*3251A>T	ENSP00000463427.1:n.*3251A>T
ENST00000584450.5:c.*40A>T	ENSP00000463714.1:n.*40A>T
ENST00000584601.5:c.3371A>T	ENSP00000462438.1:p.Glu1124Val
NM_001005862.2:c.3371A>T , LRG_724t1:c.3371A>T	NP_001005862.1:p.Glu1124Val
NM_001289936.1:c.3416A>T , LRG_724t4:c.3416A>T	NP_001276865.1:p.Glu1139Val
NM_001289937.1:c.*40A>T	NP_001276866.1:n.*40A>T
NM_004448.3:c.3461A>T , LRG_724t2:c.3461A>T	NP_004439.2:p.Glu1154Val
NR_110535.1:n.3785A>T
XM_024450641.1:c.3599A>T	XP_024306409.1:p.Glu1200Val
XM_024450642.1:c.3554A>T	XP_024306410.1:p.Glu1185Val
XM_024450643.1:c.3509A>T	XP_024306411.1:p.Glu1170Val
NM_001005862.3:c.3371A>T	NP_001005862.1:p.Glu1124Val
NM_001289936.2:c.3416A>T	NP_001276865.1:p.Glu1139Val
NM_001289937.2:c.*40A>T	NP_001276866.1:n.*40A>T
NM_001382782.1:c.3371A>T	NP_001369711.1:p.Glu1124Val
NM_001382783.1:c.3371A>T	NP_001369712.1:p.Glu1124Val
NM_001382784.1:c.3578A>T	NP_001369713.1:p.Glu1193Val
NM_001382785.1:c.3563A>T	NP_001369714.1:p.Glu1188Val
NM_001382786.1:c.3542A>T	NP_001369715.1:p.Glu1181Val
NM_001382787.1:c.3536A>T	NP_001369716.1:p.Glu1179Val
NM_001382788.1:c.3491A>T	NP_001369717.1:p.Glu1164Val
NM_001382789.1:c.3482A>T	NP_001369718.1:p.Glu1161Val
NM_001382790.1:c.3458A>T	NP_001369719.1:p.Glu1153Val
NM_001382791.1:c.3452A>T	NP_001369720.1:p.Glu1151Val
NM_001382792.1:c.3425A>T	NP_001369721.1:p.Glu1142Val
NM_001382793.1:c.3419A>T	NP_001369722.1:p.Glu1140Val
NM_001382794.1:c.3419A>T	NP_001369723.1:p.Glu1140Val
NM_001382795.1:c.3413A>T	NP_001369724.1:p.Glu1138Val
NM_001382796.1:c.3374A>T	NP_001369725.1:p.Glu1125Val
NM_001382797.1:c.3362A>T	NP_001369726.1:p.Glu1121Val
NM_001382798.1:c.3305A>T	NP_001369727.1:p.Glu1102Val
NM_001382799.1:c.3281A>T	NP_001369728.1:p.Glu1094Val
NM_001382800.1:c.3275A>T	NP_001369729.1:p.Glu1092Val
NM_001382801.1:c.3257A>T	NP_001369730.1:p.Glu1086Val
NM_001382802.1:c.3203A>T	NP_001369731.1:p.Glu1068Val
NM_001382803.1:c.*40A>T	NP_001369732.1:n.*40A>T
NM_001382804.1:c.2633A>T	NP_001369733.1:p.Glu878Val
NM_001382805.1:c.2510A>T	NP_001369734.1:p.Glu837Val
NM_001382806.1:c.2423A>T	NP_001369735.1:p.Glu808Val
NM_004448.4:c.3461A>T MANE Select	NP_004439.2:p.Glu1154Val
NR_110535.2:n.3699A>T