Canonical Allele Identifier: CA399312919

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3461A>C MANE Select	ENSP00000269571.4:p.Glu1154Ala
ENST00000269571.9:c.3461A>C	ENSP00000269571.4:p.Glu1154Ala
ENST00000406381.6:c.3371A>C	ENSP00000385185.2:p.Glu1124Ala
ENST00000445658.6:c.2633A>C	ENSP00000404047.2:p.Glu878Ala
ENST00000541774.5:c.3416A>C	ENSP00000446466.1:p.Glu1139Ala
ENST00000578373.5:c.*3251A>C	ENSP00000463427.1:n.*3251A>C
ENST00000584450.5:c.*40A>C	ENSP00000463714.1:n.*40A>C
ENST00000584601.5:c.3371A>C	ENSP00000462438.1:p.Glu1124Ala
NM_001005862.2:c.3371A>C , LRG_724t1:c.3371A>C	NP_001005862.1:p.Glu1124Ala
NM_001289936.1:c.3416A>C , LRG_724t4:c.3416A>C	NP_001276865.1:p.Glu1139Ala
NM_001289937.1:c.*40A>C	NP_001276866.1:n.*40A>C
NM_004448.3:c.3461A>C , LRG_724t2:c.3461A>C	NP_004439.2:p.Glu1154Ala
NR_110535.1:n.3785A>C
XM_024450641.1:c.3599A>C	XP_024306409.1:p.Glu1200Ala
XM_024450642.1:c.3554A>C	XP_024306410.1:p.Glu1185Ala
XM_024450643.1:c.3509A>C	XP_024306411.1:p.Glu1170Ala
NM_001005862.3:c.3371A>C	NP_001005862.1:p.Glu1124Ala
NM_001289936.2:c.3416A>C	NP_001276865.1:p.Glu1139Ala
NM_001289937.2:c.*40A>C	NP_001276866.1:n.*40A>C
NM_001382782.1:c.3371A>C	NP_001369711.1:p.Glu1124Ala
NM_001382783.1:c.3371A>C	NP_001369712.1:p.Glu1124Ala
NM_001382784.1:c.3578A>C	NP_001369713.1:p.Glu1193Ala
NM_001382785.1:c.3563A>C	NP_001369714.1:p.Glu1188Ala
NM_001382786.1:c.3542A>C	NP_001369715.1:p.Glu1181Ala
NM_001382787.1:c.3536A>C	NP_001369716.1:p.Glu1179Ala
NM_001382788.1:c.3491A>C	NP_001369717.1:p.Glu1164Ala
NM_001382789.1:c.3482A>C	NP_001369718.1:p.Glu1161Ala
NM_001382790.1:c.3458A>C	NP_001369719.1:p.Glu1153Ala
NM_001382791.1:c.3452A>C	NP_001369720.1:p.Glu1151Ala
NM_001382792.1:c.3425A>C	NP_001369721.1:p.Glu1142Ala
NM_001382793.1:c.3419A>C	NP_001369722.1:p.Glu1140Ala
NM_001382794.1:c.3419A>C	NP_001369723.1:p.Glu1140Ala
NM_001382795.1:c.3413A>C	NP_001369724.1:p.Glu1138Ala
NM_001382796.1:c.3374A>C	NP_001369725.1:p.Glu1125Ala
NM_001382797.1:c.3362A>C	NP_001369726.1:p.Glu1121Ala
NM_001382798.1:c.3305A>C	NP_001369727.1:p.Glu1102Ala
NM_001382799.1:c.3281A>C	NP_001369728.1:p.Glu1094Ala
NM_001382800.1:c.3275A>C	NP_001369729.1:p.Glu1092Ala
NM_001382801.1:c.3257A>C	NP_001369730.1:p.Glu1086Ala
NM_001382802.1:c.3203A>C	NP_001369731.1:p.Glu1068Ala
NM_001382803.1:c.*40A>C	NP_001369732.1:n.*40A>C
NM_001382804.1:c.2633A>C	NP_001369733.1:p.Glu878Ala
NM_001382805.1:c.2510A>C	NP_001369734.1:p.Glu837Ala
NM_001382806.1:c.2423A>C	NP_001369735.1:p.Glu808Ala
NM_004448.4:c.3461A>C MANE Select	NP_004439.2:p.Glu1154Ala
NR_110535.2:n.3699A>C