Canonical Allele Identifier: CA399310548

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143242841
• MyVariant Identifiers: chr17:g.37883642T>A (hg19) ; chr17:g.39727389T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727389T>A , CM000679.2:g.39727389T>A	GRCh38
NC_000017.10:g.37883642T>A , CM000679.1:g.37883642T>A	GRCh37
NC_000017.9:g.35137168T>A	NCBI36
NG_007503.1:g.44250T>A , LRG_724:g.44250T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3254T>A MANE Select	ENSP00000269571.4:p.Val1085Glu
ENST00000269571.9:c.3254T>A	ENSP00000269571.4:p.Val1085Glu
ENST00000406381.6:c.3164T>A	ENSP00000385185.2:p.Val1055Glu
ENST00000445658.6:c.2426T>A	ENSP00000404047.2:p.Val809Glu
ENST00000541774.5:c.3209T>A	ENSP00000446466.1:p.Val1070Glu
ENST00000578373.5:c.*3044T>A	ENSP00000463427.1:n.*3044T>A
ENST00000584450.5:c.3160-300T>A	ENSP00000463714.1:n.3160-300T>A
ENST00000584601.5:c.3164T>A	ENSP00000462438.1:p.Val1055Glu
NM_001005862.2:c.3164T>A , LRG_724t1:c.3164T>A	NP_001005862.1:p.Val1055Glu
NM_001289936.1:c.3209T>A , LRG_724t4:c.3209T>A	NP_001276865.1:p.Val1070Glu
NM_001289937.1:c.3160-300T>A	NP_001276866.1:n.3160-300T>A
NM_004448.3:c.3254T>A , LRG_724t2:c.3254T>A	NP_004439.2:p.Val1085Glu
NR_110535.1:n.3578T>A
XM_024450641.1:c.3392T>A	XP_024306409.1:p.Val1131Glu
XM_024450642.1:c.3347T>A	XP_024306410.1:p.Val1116Glu
XM_024450643.1:c.3302T>A	XP_024306411.1:p.Val1101Glu
NM_001005862.3:c.3164T>A	NP_001005862.1:p.Val1055Glu
NM_001289936.2:c.3209T>A	NP_001276865.1:p.Val1070Glu
NM_001289937.2:c.3160-300T>A	NP_001276866.1:n.3160-300T>A
NM_001382782.1:c.3164T>A	NP_001369711.1:p.Val1055Glu
NM_001382783.1:c.3164T>A	NP_001369712.1:p.Val1055Glu
NM_001382784.1:c.3371T>A	NP_001369713.1:p.Val1124Glu
NM_001382785.1:c.3356T>A	NP_001369714.1:p.Val1119Glu
NM_001382786.1:c.3335T>A	NP_001369715.1:p.Val1112Glu
NM_001382787.1:c.3329T>A	NP_001369716.1:p.Val1110Glu
NM_001382788.1:c.3284T>A	NP_001369717.1:p.Val1095Glu
NM_001382789.1:c.3275T>A	NP_001369718.1:p.Val1092Glu
NM_001382790.1:c.3251T>A	NP_001369719.1:p.Val1084Glu
NM_001382791.1:c.3245T>A	NP_001369720.1:p.Val1082Glu
NM_001382792.1:c.3218T>A	NP_001369721.1:p.Val1073Glu
NM_001382793.1:c.3212T>A	NP_001369722.1:p.Val1071Glu
NM_001382794.1:c.3212T>A	NP_001369723.1:p.Val1071Glu
NM_001382795.1:c.3206T>A	NP_001369724.1:p.Val1069Glu
NM_001382796.1:c.3167T>A	NP_001369725.1:p.Val1056Glu
NM_001382797.1:c.3155T>A	NP_001369726.1:p.Val1052Glu
NM_001382798.1:c.3098T>A	NP_001369727.1:p.Val1033Glu
NM_001382799.1:c.3074T>A	NP_001369728.1:p.Val1025Glu
NM_001382800.1:c.3068T>A	NP_001369729.1:p.Val1023Glu
NM_001382801.1:c.3050T>A	NP_001369730.1:p.Val1017Glu
NM_001382802.1:c.2996T>A	NP_001369731.1:p.Val999Glu
NM_001382803.1:c.3118-300T>A	NP_001369732.1:n.3118-300T>A
NM_001382804.1:c.2426T>A	NP_001369733.1:p.Val809Glu
NM_001382805.1:c.2303T>A	NP_001369734.1:p.Val768Glu
NM_001382806.1:c.2216T>A	NP_001369735.1:p.Val739Glu
NM_004448.4:c.3254T>A MANE Select	NP_004439.2:p.Val1085Glu
NR_110535.2:n.3492T>A