Canonical Allele Identifier: CA399314485

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884206A>C (hg19) ; chr17:g.39727953A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727953A>C , CM000679.2:g.39727953A>C	GRCh38
NC_000017.10:g.37884206A>C , CM000679.1:g.37884206A>C	GRCh37
NC_000017.9:g.35137732A>C	NCBI36
NG_007503.1:g.44814A>C , LRG_724:g.44814A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3677A>C MANE Select	ENSP00000269571.4:p.Asp1226Ala
ENST00000269571.9:c.3677A>C	ENSP00000269571.4:p.Asp1226Ala
ENST00000406381.6:c.3587A>C	ENSP00000385185.2:p.Asp1196Ala
ENST00000445658.6:c.2849A>C	ENSP00000404047.2:p.Asp950Ala
ENST00000541774.5:c.3632A>C	ENSP00000446466.1:p.Asp1211Ala
ENST00000578373.5:c.*3467A>C	ENSP00000463427.1:n.*3467A>C
ENST00000584450.5:c.*256A>C	ENSP00000463714.1:n.*256A>C
ENST00000584601.5:c.3587A>C	ENSP00000462438.1:p.Asp1196Ala
NM_001005862.2:c.3587A>C , LRG_724t1:c.3587A>C	NP_001005862.1:p.Asp1196Ala
NM_001289936.1:c.3632A>C , LRG_724t4:c.3632A>C	NP_001276865.1:p.Asp1211Ala
NM_001289937.1:c.*256A>C	NP_001276866.1:n.*256A>C
NM_004448.3:c.3677A>C , LRG_724t2:c.3677A>C	NP_004439.2:p.Asp1226Ala
NR_110535.1:n.4001A>C
XM_024450641.1:c.3815A>C	XP_024306409.1:p.Asp1272Ala
XM_024450642.1:c.3770A>C	XP_024306410.1:p.Asp1257Ala
XM_024450643.1:c.3725A>C	XP_024306411.1:p.Asp1242Ala
NM_001005862.3:c.3587A>C	NP_001005862.1:p.Asp1196Ala
NM_001289936.2:c.3632A>C	NP_001276865.1:p.Asp1211Ala
NM_001289937.2:c.*256A>C	NP_001276866.1:n.*256A>C
NM_001382782.1:c.3587A>C	NP_001369711.1:p.Asp1196Ala
NM_001382783.1:c.3587A>C	NP_001369712.1:p.Asp1196Ala
NM_001382784.1:c.3794A>C	NP_001369713.1:p.Asp1265Ala
NM_001382785.1:c.3779A>C	NP_001369714.1:p.Asp1260Ala
NM_001382786.1:c.3758A>C	NP_001369715.1:p.Asp1253Ala
NM_001382787.1:c.3752A>C	NP_001369716.1:p.Asp1251Ala
NM_001382788.1:c.3707A>C	NP_001369717.1:p.Asp1236Ala
NM_001382789.1:c.3698A>C	NP_001369718.1:p.Asp1233Ala
NM_001382790.1:c.3674A>C	NP_001369719.1:p.Asp1225Ala
NM_001382791.1:c.3668A>C	NP_001369720.1:p.Asp1223Ala
NM_001382792.1:c.3641A>C	NP_001369721.1:p.Asp1214Ala
NM_001382793.1:c.3635A>C	NP_001369722.1:p.Asp1212Ala
NM_001382794.1:c.3635A>C	NP_001369723.1:p.Asp1212Ala
NM_001382795.1:c.3629A>C	NP_001369724.1:p.Asp1210Ala
NM_001382796.1:c.3590A>C	NP_001369725.1:p.Asp1197Ala
NM_001382797.1:c.3578A>C	NP_001369726.1:p.Asp1193Ala
NM_001382798.1:c.3521A>C	NP_001369727.1:p.Asp1174Ala
NM_001382799.1:c.3497A>C	NP_001369728.1:p.Asp1166Ala
NM_001382800.1:c.3491A>C	NP_001369729.1:p.Asp1164Ala
NM_001382801.1:c.3473A>C	NP_001369730.1:p.Asp1158Ala
NM_001382802.1:c.3419A>C	NP_001369731.1:p.Asp1140Ala
NM_001382803.1:c.*256A>C	NP_001369732.1:n.*256A>C
NM_001382804.1:c.2849A>C	NP_001369733.1:p.Asp950Ala
NM_001382805.1:c.2726A>C	NP_001369734.1:p.Asp909Ala
NM_001382806.1:c.2639A>C	NP_001369735.1:p.Asp880Ala
NM_004448.4:c.3677A>C MANE Select	NP_004439.2:p.Asp1226Ala
NR_110535.2:n.3915A>C