Canonical Allele Identifier: CA399310685

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143245983
• MyVariant Identifiers: chr17:g.37883669C>A (hg19) ; chr17:g.39727416C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727416C>A , CM000679.2:g.39727416C>A	GRCh38
NC_000017.10:g.37883669C>A , CM000679.1:g.37883669C>A	GRCh37
NC_000017.9:g.35137195C>A	NCBI36
NG_007503.1:g.44277C>A , LRG_724:g.44277C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3281C>A MANE Select	ENSP00000269571.4:p.Ala1094Glu
ENST00000269571.9:c.3281C>A	ENSP00000269571.4:p.Ala1094Glu
ENST00000406381.6:c.3191C>A	ENSP00000385185.2:p.Ala1064Glu
ENST00000445658.6:c.2453C>A	ENSP00000404047.2:p.Ala818Glu
ENST00000541774.5:c.3236C>A	ENSP00000446466.1:p.Ala1079Glu
ENST00000578373.5:c.*3071C>A	ENSP00000463427.1:n.*3071C>A
ENST00000584450.5:c.3160-273C>A	ENSP00000463714.1:n.3160-273C>A
ENST00000584601.5:c.3191C>A	ENSP00000462438.1:p.Ala1064Glu
NM_001005862.2:c.3191C>A , LRG_724t1:c.3191C>A	NP_001005862.1:p.Ala1064Glu
NM_001289936.1:c.3236C>A , LRG_724t4:c.3236C>A	NP_001276865.1:p.Ala1079Glu
NM_001289937.1:c.3160-273C>A	NP_001276866.1:n.3160-273C>A
NM_004448.3:c.3281C>A , LRG_724t2:c.3281C>A	NP_004439.2:p.Ala1094Glu
NR_110535.1:n.3605C>A
XM_024450641.1:c.3419C>A	XP_024306409.1:p.Ala1140Glu
XM_024450642.1:c.3374C>A	XP_024306410.1:p.Ala1125Glu
XM_024450643.1:c.3329C>A	XP_024306411.1:p.Ala1110Glu
NM_001005862.3:c.3191C>A	NP_001005862.1:p.Ala1064Glu
NM_001289936.2:c.3236C>A	NP_001276865.1:p.Ala1079Glu
NM_001289937.2:c.3160-273C>A	NP_001276866.1:n.3160-273C>A
NM_001382782.1:c.3191C>A	NP_001369711.1:p.Ala1064Glu
NM_001382783.1:c.3191C>A	NP_001369712.1:p.Ala1064Glu
NM_001382784.1:c.3398C>A	NP_001369713.1:p.Ala1133Glu
NM_001382785.1:c.3383C>A	NP_001369714.1:p.Ala1128Glu
NM_001382786.1:c.3362C>A	NP_001369715.1:p.Ala1121Glu
NM_001382787.1:c.3356C>A	NP_001369716.1:p.Ala1119Glu
NM_001382788.1:c.3311C>A	NP_001369717.1:p.Ala1104Glu
NM_001382789.1:c.3302C>A	NP_001369718.1:p.Ala1101Glu
NM_001382790.1:c.3278C>A	NP_001369719.1:p.Ala1093Glu
NM_001382791.1:c.3272C>A	NP_001369720.1:p.Ala1091Glu
NM_001382792.1:c.3245C>A	NP_001369721.1:p.Ala1082Glu
NM_001382793.1:c.3239C>A	NP_001369722.1:p.Ala1080Glu
NM_001382794.1:c.3239C>A	NP_001369723.1:p.Ala1080Glu
NM_001382795.1:c.3233C>A	NP_001369724.1:p.Ala1078Glu
NM_001382796.1:c.3194C>A	NP_001369725.1:p.Ala1065Glu
NM_001382797.1:c.3182C>A	NP_001369726.1:p.Ala1061Glu
NM_001382798.1:c.3125C>A	NP_001369727.1:p.Ala1042Glu
NM_001382799.1:c.3101C>A	NP_001369728.1:p.Ala1034Glu
NM_001382800.1:c.3095C>A	NP_001369729.1:p.Ala1032Glu
NM_001382801.1:c.3077C>A	NP_001369730.1:p.Ala1026Glu
NM_001382802.1:c.3023C>A	NP_001369731.1:p.Ala1008Glu
NM_001382803.1:c.3118-273C>A	NP_001369732.1:n.3118-273C>A
NM_001382804.1:c.2453C>A	NP_001369733.1:p.Ala818Glu
NM_001382805.1:c.2330C>A	NP_001369734.1:p.Ala777Glu
NM_001382806.1:c.2243C>A	NP_001369735.1:p.Ala748Glu
NM_004448.4:c.3281C>A MANE Select	NP_004439.2:p.Ala1094Glu
NR_110535.2:n.3519C>A