Canonical Allele Identifier: CA399310551

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883642T>C (hg19) ; chr17:g.39727389T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3254T>C MANE Select	ENSP00000269571.4:p.Val1085Ala
ENST00000269571.9:c.3254T>C	ENSP00000269571.4:p.Val1085Ala
ENST00000406381.6:c.3164T>C	ENSP00000385185.2:p.Val1055Ala
ENST00000445658.6:c.2426T>C	ENSP00000404047.2:p.Val809Ala
ENST00000541774.5:c.3209T>C	ENSP00000446466.1:p.Val1070Ala
ENST00000578373.5:c.*3044T>C	ENSP00000463427.1:n.*3044T>C
ENST00000584450.5:c.3160-300T>C	ENSP00000463714.1:n.3160-300T>C
ENST00000584601.5:c.3164T>C	ENSP00000462438.1:p.Val1055Ala
NM_001005862.2:c.3164T>C , LRG_724t1:c.3164T>C	NP_001005862.1:p.Val1055Ala
NM_001289936.1:c.3209T>C , LRG_724t4:c.3209T>C	NP_001276865.1:p.Val1070Ala
NM_001289937.1:c.3160-300T>C	NP_001276866.1:n.3160-300T>C
NM_004448.3:c.3254T>C , LRG_724t2:c.3254T>C	NP_004439.2:p.Val1085Ala
NR_110535.1:n.3578T>C
XM_024450641.1:c.3392T>C	XP_024306409.1:p.Val1131Ala
XM_024450642.1:c.3347T>C	XP_024306410.1:p.Val1116Ala
XM_024450643.1:c.3302T>C	XP_024306411.1:p.Val1101Ala
NM_001005862.3:c.3164T>C	NP_001005862.1:p.Val1055Ala
NM_001289936.2:c.3209T>C	NP_001276865.1:p.Val1070Ala
NM_001289937.2:c.3160-300T>C	NP_001276866.1:n.3160-300T>C
NM_001382782.1:c.3164T>C	NP_001369711.1:p.Val1055Ala
NM_001382783.1:c.3164T>C	NP_001369712.1:p.Val1055Ala
NM_001382784.1:c.3371T>C	NP_001369713.1:p.Val1124Ala
NM_001382785.1:c.3356T>C	NP_001369714.1:p.Val1119Ala
NM_001382786.1:c.3335T>C	NP_001369715.1:p.Val1112Ala
NM_001382787.1:c.3329T>C	NP_001369716.1:p.Val1110Ala
NM_001382788.1:c.3284T>C	NP_001369717.1:p.Val1095Ala
NM_001382789.1:c.3275T>C	NP_001369718.1:p.Val1092Ala
NM_001382790.1:c.3251T>C	NP_001369719.1:p.Val1084Ala
NM_001382791.1:c.3245T>C	NP_001369720.1:p.Val1082Ala
NM_001382792.1:c.3218T>C	NP_001369721.1:p.Val1073Ala
NM_001382793.1:c.3212T>C	NP_001369722.1:p.Val1071Ala
NM_001382794.1:c.3212T>C	NP_001369723.1:p.Val1071Ala
NM_001382795.1:c.3206T>C	NP_001369724.1:p.Val1069Ala
NM_001382796.1:c.3167T>C	NP_001369725.1:p.Val1056Ala
NM_001382797.1:c.3155T>C	NP_001369726.1:p.Val1052Ala
NM_001382798.1:c.3098T>C	NP_001369727.1:p.Val1033Ala
NM_001382799.1:c.3074T>C	NP_001369728.1:p.Val1025Ala
NM_001382800.1:c.3068T>C	NP_001369729.1:p.Val1023Ala
NM_001382801.1:c.3050T>C	NP_001369730.1:p.Val1017Ala
NM_001382802.1:c.2996T>C	NP_001369731.1:p.Val999Ala
NM_001382803.1:c.3118-300T>C	NP_001369732.1:n.3118-300T>C
NM_001382804.1:c.2426T>C	NP_001369733.1:p.Val809Ala
NM_001382805.1:c.2303T>C	NP_001369734.1:p.Val768Ala
NM_001382806.1:c.2216T>C	NP_001369735.1:p.Val739Ala
NM_004448.4:c.3254T>C MANE Select	NP_004439.2:p.Val1085Ala
NR_110535.2:n.3492T>C