Canonical Allele Identifier: CA499890491

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143288573
• MyVariant Identifiers: chr17:g.37883964T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727711T>A , CM000679.2:g.39727711T>A	GRCh38
NC_000017.10:g.37883964T>A , CM000679.1:g.37883964T>A	GRCh37
NC_000017.9:g.35137490T>A	NCBI36
NG_007503.1:g.44572T>A , LRG_724:g.44572T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3435T>A MANE Select	ENSP00000269571.4:p.Val1145=
ENST00000269571.9:c.3435T>A	ENSP00000269571.4:p.Val1145=
ENST00000406381.6:c.3345T>A	ENSP00000385185.2:p.Val1115=
ENST00000445658.6:c.2607T>A	ENSP00000404047.2:p.Val869=
ENST00000541774.5:c.3390T>A	ENSP00000446466.1:p.Val1130=
ENST00000578373.5:c.*3225T>A	ENSP00000463427.1:n.*3225T>A
ENST00000584450.5:c.*14T>A	ENSP00000463714.1:n.*14T>A
ENST00000584601.5:c.3345T>A	ENSP00000462438.1:p.Val1115=
NM_001005862.2:c.3345T>A , LRG_724t1:c.3345T>A	NP_001005862.1:p.Val1115=
NM_001289936.1:c.3390T>A , LRG_724t4:c.3390T>A	NP_001276865.1:p.Val1130=
NM_001289937.1:c.*14T>A	NP_001276866.1:n.*14T>A
NM_004448.3:c.3435T>A , LRG_724t2:c.3435T>A	NP_004439.2:p.Val1145=
NR_110535.1:n.3759T>A
XM_024450641.1:c.3573T>A	XP_024306409.1:p.Val1191=
XM_024450642.1:c.3528T>A	XP_024306410.1:p.Val1176=
XM_024450643.1:c.3483T>A	XP_024306411.1:p.Val1161=
NM_001005862.3:c.3345T>A	NP_001005862.1:p.Val1115=
NM_001289936.2:c.3390T>A	NP_001276865.1:p.Val1130=
NM_001289937.2:c.*14T>A	NP_001276866.1:n.*14T>A
NM_001382782.1:c.3345T>A	NP_001369711.1:p.Val1115=
NM_001382783.1:c.3345T>A	NP_001369712.1:p.Val1115=
NM_001382784.1:c.3552T>A	NP_001369713.1:p.Val1184=
NM_001382785.1:c.3537T>A	NP_001369714.1:p.Val1179=
NM_001382786.1:c.3516T>A	NP_001369715.1:p.Val1172=
NM_001382787.1:c.3510T>A	NP_001369716.1:p.Val1170=
NM_001382788.1:c.3465T>A	NP_001369717.1:p.Val1155=
NM_001382789.1:c.3456T>A	NP_001369718.1:p.Val1152=
NM_001382790.1:c.3432T>A	NP_001369719.1:p.Val1144=
NM_001382791.1:c.3426T>A	NP_001369720.1:p.Val1142=
NM_001382792.1:c.3399T>A	NP_001369721.1:p.Val1133=
NM_001382793.1:c.3393T>A	NP_001369722.1:p.Val1131=
NM_001382794.1:c.3393T>A	NP_001369723.1:p.Val1131=
NM_001382795.1:c.3387T>A	NP_001369724.1:p.Val1129=
NM_001382796.1:c.3348T>A	NP_001369725.1:p.Val1116=
NM_001382797.1:c.3336T>A	NP_001369726.1:p.Val1112=
NM_001382798.1:c.3279T>A	NP_001369727.1:p.Val1093=
NM_001382799.1:c.3255T>A	NP_001369728.1:p.Val1085=
NM_001382800.1:c.3249T>A	NP_001369729.1:p.Val1083=
NM_001382801.1:c.3231T>A	NP_001369730.1:p.Val1077=
NM_001382802.1:c.3177T>A	NP_001369731.1:p.Val1059=
NM_001382803.1:c.*14T>A	NP_001369732.1:n.*14T>A
NM_001382804.1:c.2607T>A	NP_001369733.1:p.Val869=
NM_001382805.1:c.2484T>A	NP_001369734.1:p.Val828=
NM_001382806.1:c.2397T>A	NP_001369735.1:p.Val799=
NM_004448.4:c.3435T>A MANE Select	NP_004439.2:p.Val1145=
NR_110535.2:n.3673T>A