Canonical Allele Identifier: CA399314546

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884215A>C (hg19) ; chr17:g.39727962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727962A>C , CM000679.2:g.39727962A>C	GRCh38
NC_000017.10:g.37884215A>C , CM000679.1:g.37884215A>C	GRCh37
NC_000017.9:g.35137741A>C	NCBI36
NG_007503.1:g.44823A>C , LRG_724:g.44823A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3686A>C MANE Select	ENSP00000269571.4:p.Glu1229Ala
ENST00000269571.9:c.3686A>C	ENSP00000269571.4:p.Glu1229Ala
ENST00000406381.6:c.3596A>C	ENSP00000385185.2:p.Glu1199Ala
ENST00000445658.6:c.2858A>C	ENSP00000404047.2:p.Glu953Ala
ENST00000541774.5:c.3641A>C	ENSP00000446466.1:p.Glu1214Ala
ENST00000578373.5:c.*3476A>C	ENSP00000463427.1:n.*3476A>C
ENST00000584450.5:c.*265A>C	ENSP00000463714.1:n.*265A>C
ENST00000584601.5:c.3596A>C	ENSP00000462438.1:p.Glu1199Ala
NM_001005862.2:c.3596A>C , LRG_724t1:c.3596A>C	NP_001005862.1:p.Glu1199Ala
NM_001289936.1:c.3641A>C , LRG_724t4:c.3641A>C	NP_001276865.1:p.Glu1214Ala
NM_001289937.1:c.*265A>C	NP_001276866.1:n.*265A>C
NM_004448.3:c.3686A>C , LRG_724t2:c.3686A>C	NP_004439.2:p.Glu1229Ala
NR_110535.1:n.4010A>C
XM_024450641.1:c.3824A>C	XP_024306409.1:p.Glu1275Ala
XM_024450642.1:c.3779A>C	XP_024306410.1:p.Glu1260Ala
XM_024450643.1:c.3734A>C	XP_024306411.1:p.Glu1245Ala
NM_001005862.3:c.3596A>C	NP_001005862.1:p.Glu1199Ala
NM_001289936.2:c.3641A>C	NP_001276865.1:p.Glu1214Ala
NM_001289937.2:c.*265A>C	NP_001276866.1:n.*265A>C
NM_001382782.1:c.3596A>C	NP_001369711.1:p.Glu1199Ala
NM_001382783.1:c.3596A>C	NP_001369712.1:p.Glu1199Ala
NM_001382784.1:c.3803A>C	NP_001369713.1:p.Glu1268Ala
NM_001382785.1:c.3788A>C	NP_001369714.1:p.Glu1263Ala
NM_001382786.1:c.3767A>C	NP_001369715.1:p.Glu1256Ala
NM_001382787.1:c.3761A>C	NP_001369716.1:p.Glu1254Ala
NM_001382788.1:c.3716A>C	NP_001369717.1:p.Glu1239Ala
NM_001382789.1:c.3707A>C	NP_001369718.1:p.Glu1236Ala
NM_001382790.1:c.3683A>C	NP_001369719.1:p.Glu1228Ala
NM_001382791.1:c.3677A>C	NP_001369720.1:p.Glu1226Ala
NM_001382792.1:c.3650A>C	NP_001369721.1:p.Glu1217Ala
NM_001382793.1:c.3644A>C	NP_001369722.1:p.Glu1215Ala
NM_001382794.1:c.3644A>C	NP_001369723.1:p.Glu1215Ala
NM_001382795.1:c.3638A>C	NP_001369724.1:p.Glu1213Ala
NM_001382796.1:c.3599A>C	NP_001369725.1:p.Glu1200Ala
NM_001382797.1:c.3587A>C	NP_001369726.1:p.Glu1196Ala
NM_001382798.1:c.3530A>C	NP_001369727.1:p.Glu1177Ala
NM_001382799.1:c.3506A>C	NP_001369728.1:p.Glu1169Ala
NM_001382800.1:c.3500A>C	NP_001369729.1:p.Glu1167Ala
NM_001382801.1:c.3482A>C	NP_001369730.1:p.Glu1161Ala
NM_001382802.1:c.3428A>C	NP_001369731.1:p.Glu1143Ala
NM_001382803.1:c.*265A>C	NP_001369732.1:n.*265A>C
NM_001382804.1:c.2858A>C	NP_001369733.1:p.Glu953Ala
NM_001382805.1:c.2735A>C	NP_001369734.1:p.Glu912Ala
NM_001382806.1:c.2648A>C	NP_001369735.1:p.Glu883Ala
NM_004448.4:c.3686A>C MANE Select	NP_004439.2:p.Glu1229Ala
NR_110535.2:n.3924A>C