Canonical Allele Identifier: CA399313077

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143294386
• MyVariant Identifiers: chr17:g.37884017C>T (hg19) ; chr17:g.39727764C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727764C>T , CM000679.2:g.39727764C>T	GRCh38
NC_000017.10:g.37884017C>T , CM000679.1:g.37884017C>T	GRCh37
NC_000017.9:g.35137543C>T	NCBI36
NG_007503.1:g.44625C>T , LRG_724:g.44625C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3488C>T MANE Select	ENSP00000269571.4:p.Ala1163Val
ENST00000269571.9:c.3488C>T	ENSP00000269571.4:p.Ala1163Val
ENST00000406381.6:c.3398C>T	ENSP00000385185.2:p.Ala1133Val
ENST00000445658.6:c.2660C>T	ENSP00000404047.2:p.Ala887Val
ENST00000541774.5:c.3443C>T	ENSP00000446466.1:p.Ala1148Val
ENST00000578373.5:c.*3278C>T	ENSP00000463427.1:n.*3278C>T
ENST00000584450.5:c.*67C>T	ENSP00000463714.1:n.*67C>T
ENST00000584601.5:c.3398C>T	ENSP00000462438.1:p.Ala1133Val
NM_001005862.2:c.3398C>T , LRG_724t1:c.3398C>T	NP_001005862.1:p.Ala1133Val
NM_001289936.1:c.3443C>T , LRG_724t4:c.3443C>T	NP_001276865.1:p.Ala1148Val
NM_001289937.1:c.*67C>T	NP_001276866.1:n.*67C>T
NM_004448.3:c.3488C>T , LRG_724t2:c.3488C>T	NP_004439.2:p.Ala1163Val
NR_110535.1:n.3812C>T
XM_024450641.1:c.3626C>T	XP_024306409.1:p.Ala1209Val
XM_024450642.1:c.3581C>T	XP_024306410.1:p.Ala1194Val
XM_024450643.1:c.3536C>T	XP_024306411.1:p.Ala1179Val
NM_001005862.3:c.3398C>T	NP_001005862.1:p.Ala1133Val
NM_001289936.2:c.3443C>T	NP_001276865.1:p.Ala1148Val
NM_001289937.2:c.*67C>T	NP_001276866.1:n.*67C>T
NM_001382782.1:c.3398C>T	NP_001369711.1:p.Ala1133Val
NM_001382783.1:c.3398C>T	NP_001369712.1:p.Ala1133Val
NM_001382784.1:c.3605C>T	NP_001369713.1:p.Ala1202Val
NM_001382785.1:c.3590C>T	NP_001369714.1:p.Ala1197Val
NM_001382786.1:c.3569C>T	NP_001369715.1:p.Ala1190Val
NM_001382787.1:c.3563C>T	NP_001369716.1:p.Ala1188Val
NM_001382788.1:c.3518C>T	NP_001369717.1:p.Ala1173Val
NM_001382789.1:c.3509C>T	NP_001369718.1:p.Ala1170Val
NM_001382790.1:c.3485C>T	NP_001369719.1:p.Ala1162Val
NM_001382791.1:c.3479C>T	NP_001369720.1:p.Ala1160Val
NM_001382792.1:c.3452C>T	NP_001369721.1:p.Ala1151Val
NM_001382793.1:c.3446C>T	NP_001369722.1:p.Ala1149Val
NM_001382794.1:c.3446C>T	NP_001369723.1:p.Ala1149Val
NM_001382795.1:c.3440C>T	NP_001369724.1:p.Ala1147Val
NM_001382796.1:c.3401C>T	NP_001369725.1:p.Ala1134Val
NM_001382797.1:c.3389C>T	NP_001369726.1:p.Ala1130Val
NM_001382798.1:c.3332C>T	NP_001369727.1:p.Ala1111Val
NM_001382799.1:c.3308C>T	NP_001369728.1:p.Ala1103Val
NM_001382800.1:c.3302C>T	NP_001369729.1:p.Ala1101Val
NM_001382801.1:c.3284C>T	NP_001369730.1:p.Ala1095Val
NM_001382802.1:c.3230C>T	NP_001369731.1:p.Ala1077Val
NM_001382803.1:c.*67C>T	NP_001369732.1:n.*67C>T
NM_001382804.1:c.2660C>T	NP_001369733.1:p.Ala887Val
NM_001382805.1:c.2537C>T	NP_001369734.1:p.Ala846Val
NM_001382806.1:c.2450C>T	NP_001369735.1:p.Ala817Val
NM_004448.4:c.3488C>T MANE Select	NP_004439.2:p.Ala1163Val
NR_110535.2:n.3726C>T