Canonical Allele Identifier: CA399312915

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143291215
• MyVariant Identifiers: chr17:g.37883989G>C (hg19) ; chr17:g.39727736G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727736G>C , CM000679.2:g.39727736G>C	GRCh38
NC_000017.10:g.37883989G>C , CM000679.1:g.37883989G>C	GRCh37
NC_000017.9:g.35137515G>C	NCBI36
NG_007503.1:g.44597G>C , LRG_724:g.44597G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3460G>C MANE Select	ENSP00000269571.4:p.Glu1154Gln
ENST00000269571.9:c.3460G>C	ENSP00000269571.4:p.Glu1154Gln
ENST00000406381.6:c.3370G>C	ENSP00000385185.2:p.Glu1124Gln
ENST00000445658.6:c.2632G>C	ENSP00000404047.2:p.Glu878Gln
ENST00000541774.5:c.3415G>C	ENSP00000446466.1:p.Glu1139Gln
ENST00000578373.5:c.*3250G>C	ENSP00000463427.1:n.*3250G>C
ENST00000584450.5:c.*39G>C	ENSP00000463714.1:n.*39G>C
ENST00000584601.5:c.3370G>C	ENSP00000462438.1:p.Glu1124Gln
NM_001005862.2:c.3370G>C , LRG_724t1:c.3370G>C	NP_001005862.1:p.Glu1124Gln
NM_001289936.1:c.3415G>C , LRG_724t4:c.3415G>C	NP_001276865.1:p.Glu1139Gln
NM_001289937.1:c.*39G>C	NP_001276866.1:n.*39G>C
NM_004448.3:c.3460G>C , LRG_724t2:c.3460G>C	NP_004439.2:p.Glu1154Gln
NR_110535.1:n.3784G>C
XM_024450641.1:c.3598G>C	XP_024306409.1:p.Glu1200Gln
XM_024450642.1:c.3553G>C	XP_024306410.1:p.Glu1185Gln
XM_024450643.1:c.3508G>C	XP_024306411.1:p.Glu1170Gln
NM_001005862.3:c.3370G>C	NP_001005862.1:p.Glu1124Gln
NM_001289936.2:c.3415G>C	NP_001276865.1:p.Glu1139Gln
NM_001289937.2:c.*39G>C	NP_001276866.1:n.*39G>C
NM_001382782.1:c.3370G>C	NP_001369711.1:p.Glu1124Gln
NM_001382783.1:c.3370G>C	NP_001369712.1:p.Glu1124Gln
NM_001382784.1:c.3577G>C	NP_001369713.1:p.Glu1193Gln
NM_001382785.1:c.3562G>C	NP_001369714.1:p.Glu1188Gln
NM_001382786.1:c.3541G>C	NP_001369715.1:p.Glu1181Gln
NM_001382787.1:c.3535G>C	NP_001369716.1:p.Glu1179Gln
NM_001382788.1:c.3490G>C	NP_001369717.1:p.Glu1164Gln
NM_001382789.1:c.3481G>C	NP_001369718.1:p.Glu1161Gln
NM_001382790.1:c.3457G>C	NP_001369719.1:p.Glu1153Gln
NM_001382791.1:c.3451G>C	NP_001369720.1:p.Glu1151Gln
NM_001382792.1:c.3424G>C	NP_001369721.1:p.Glu1142Gln
NM_001382793.1:c.3418G>C	NP_001369722.1:p.Glu1140Gln
NM_001382794.1:c.3418G>C	NP_001369723.1:p.Glu1140Gln
NM_001382795.1:c.3412G>C	NP_001369724.1:p.Glu1138Gln
NM_001382796.1:c.3373G>C	NP_001369725.1:p.Glu1125Gln
NM_001382797.1:c.3361G>C	NP_001369726.1:p.Glu1121Gln
NM_001382798.1:c.3304G>C	NP_001369727.1:p.Glu1102Gln
NM_001382799.1:c.3280G>C	NP_001369728.1:p.Glu1094Gln
NM_001382800.1:c.3274G>C	NP_001369729.1:p.Glu1092Gln
NM_001382801.1:c.3256G>C	NP_001369730.1:p.Glu1086Gln
NM_001382802.1:c.3202G>C	NP_001369731.1:p.Glu1068Gln
NM_001382803.1:c.*39G>C	NP_001369732.1:n.*39G>C
NM_001382804.1:c.2632G>C	NP_001369733.1:p.Glu878Gln
NM_001382805.1:c.2509G>C	NP_001369734.1:p.Glu837Gln
NM_001382806.1:c.2422G>C	NP_001369735.1:p.Glu808Gln
NM_004448.4:c.3460G>C MANE Select	NP_004439.2:p.Glu1154Gln
NR_110535.2:n.3698G>C