Canonical Allele Identifier: CA499890282

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883772T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727519T>A , CM000679.2:g.39727519T>A	GRCh38
NC_000017.10:g.37883772T>A , CM000679.1:g.37883772T>A	GRCh37
NC_000017.9:g.35137298T>A	NCBI36
NG_007503.1:g.44380T>A , LRG_724:g.44380T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3384T>A MANE Select	ENSP00000269571.4:p.Val1128=
ENST00000269571.9:c.3384T>A	ENSP00000269571.4:p.Val1128=
ENST00000406381.6:c.3294T>A	ENSP00000385185.2:p.Val1098=
ENST00000445658.6:c.2556T>A	ENSP00000404047.2:p.Val852=
ENST00000541774.5:c.3339T>A	ENSP00000446466.1:p.Val1113=
ENST00000578373.5:c.*3174T>A	ENSP00000463427.1:n.*3174T>A
ENST00000584450.5:c.3160-170T>A	ENSP00000463714.1:n.3160-170T>A
ENST00000584601.5:c.3294T>A	ENSP00000462438.1:p.Val1098=
NM_001005862.2:c.3294T>A , LRG_724t1:c.3294T>A	NP_001005862.1:p.Val1098=
NM_001289936.1:c.3339T>A , LRG_724t4:c.3339T>A	NP_001276865.1:p.Val1113=
NM_001289937.1:c.3160-170T>A	NP_001276866.1:n.3160-170T>A
NM_004448.3:c.3384T>A , LRG_724t2:c.3384T>A	NP_004439.2:p.Val1128=
NR_110535.1:n.3708T>A
XM_024450641.1:c.3522T>A	XP_024306409.1:p.Val1174=
XM_024450642.1:c.3477T>A	XP_024306410.1:p.Val1159=
XM_024450643.1:c.3432T>A	XP_024306411.1:p.Val1144=
NM_001005862.3:c.3294T>A	NP_001005862.1:p.Val1098=
NM_001289936.2:c.3339T>A	NP_001276865.1:p.Val1113=
NM_001289937.2:c.3160-170T>A	NP_001276866.1:n.3160-170T>A
NM_001382782.1:c.3294T>A	NP_001369711.1:p.Val1098=
NM_001382783.1:c.3294T>A	NP_001369712.1:p.Val1098=
NM_001382784.1:c.3501T>A	NP_001369713.1:p.Val1167=
NM_001382785.1:c.3486T>A	NP_001369714.1:p.Val1162=
NM_001382786.1:c.3465T>A	NP_001369715.1:p.Val1155=
NM_001382787.1:c.3459T>A	NP_001369716.1:p.Val1153=
NM_001382788.1:c.3414T>A	NP_001369717.1:p.Val1138=
NM_001382789.1:c.3405T>A	NP_001369718.1:p.Val1135=
NM_001382790.1:c.3381T>A	NP_001369719.1:p.Val1127=
NM_001382791.1:c.3375T>A	NP_001369720.1:p.Val1125=
NM_001382792.1:c.3348T>A	NP_001369721.1:p.Val1116=
NM_001382793.1:c.3342T>A	NP_001369722.1:p.Val1114=
NM_001382794.1:c.3342T>A	NP_001369723.1:p.Val1114=
NM_001382795.1:c.3336T>A	NP_001369724.1:p.Val1112=
NM_001382796.1:c.3297T>A	NP_001369725.1:p.Val1099=
NM_001382797.1:c.3285T>A	NP_001369726.1:p.Val1095=
NM_001382798.1:c.3228T>A	NP_001369727.1:p.Val1076=
NM_001382799.1:c.3204T>A	NP_001369728.1:p.Val1068=
NM_001382800.1:c.3198T>A	NP_001369729.1:p.Val1066=
NM_001382801.1:c.3180T>A	NP_001369730.1:p.Val1060=
NM_001382802.1:c.3126T>A	NP_001369731.1:p.Val1042=
NM_001382803.1:c.3118-170T>A	NP_001369732.1:n.3118-170T>A
NM_001382804.1:c.2556T>A	NP_001369733.1:p.Val852=
NM_001382805.1:c.2433T>A	NP_001369734.1:p.Val811=
NM_001382806.1:c.2346T>A	NP_001369735.1:p.Val782=
NM_004448.4:c.3384T>A MANE Select	NP_004439.2:p.Val1128=
NR_110535.2:n.3622T>A