Canonical Allele Identifier: CA399310440

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883625A>C (hg19) ; chr17:g.39727372A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727372A>C , CM000679.2:g.39727372A>C	GRCh38
NC_000017.10:g.37883625A>C , CM000679.1:g.37883625A>C	GRCh37
NC_000017.9:g.35137151A>C	NCBI36
NG_007503.1:g.44233A>C , LRG_724:g.44233A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3237A>C MANE Select	ENSP00000269571.4:p.Glu1079Asp
ENST00000269571.9:c.3237A>C	ENSP00000269571.4:p.Glu1079Asp
ENST00000406381.6:c.3147A>C	ENSP00000385185.2:p.Glu1049Asp
ENST00000445658.6:c.2409A>C	ENSP00000404047.2:p.Glu803Asp
ENST00000541774.5:c.3192A>C	ENSP00000446466.1:p.Glu1064Asp
ENST00000578373.5:c.*3027A>C	ENSP00000463427.1:n.*3027A>C
ENST00000584450.5:c.3160-317A>C	ENSP00000463714.1:n.3160-317A>C
ENST00000584601.5:c.3147A>C	ENSP00000462438.1:p.Glu1049Asp
NM_001005862.2:c.3147A>C , LRG_724t1:c.3147A>C	NP_001005862.1:p.Glu1049Asp
NM_001289936.1:c.3192A>C , LRG_724t4:c.3192A>C	NP_001276865.1:p.Glu1064Asp
NM_001289937.1:c.3160-317A>C	NP_001276866.1:n.3160-317A>C
NM_004448.3:c.3237A>C , LRG_724t2:c.3237A>C	NP_004439.2:p.Glu1079Asp
NR_110535.1:n.3561A>C
XM_024450641.1:c.3375A>C	XP_024306409.1:p.Glu1125Asp
XM_024450642.1:c.3330A>C	XP_024306410.1:p.Glu1110Asp
XM_024450643.1:c.3285A>C	XP_024306411.1:p.Glu1095Asp
NM_001005862.3:c.3147A>C	NP_001005862.1:p.Glu1049Asp
NM_001289936.2:c.3192A>C	NP_001276865.1:p.Glu1064Asp
NM_001289937.2:c.3160-317A>C	NP_001276866.1:n.3160-317A>C
NM_001382782.1:c.3147A>C	NP_001369711.1:p.Glu1049Asp
NM_001382783.1:c.3147A>C	NP_001369712.1:p.Glu1049Asp
NM_001382784.1:c.3354A>C	NP_001369713.1:p.Glu1118Asp
NM_001382785.1:c.3339A>C	NP_001369714.1:p.Glu1113Asp
NM_001382786.1:c.3318A>C	NP_001369715.1:p.Glu1106Asp
NM_001382787.1:c.3312A>C	NP_001369716.1:p.Glu1104Asp
NM_001382788.1:c.3267A>C	NP_001369717.1:p.Glu1089Asp
NM_001382789.1:c.3258A>C	NP_001369718.1:p.Glu1086Asp
NM_001382790.1:c.3234A>C	NP_001369719.1:p.Glu1078Asp
NM_001382791.1:c.3228A>C	NP_001369720.1:p.Glu1076Asp
NM_001382792.1:c.3201A>C	NP_001369721.1:p.Glu1067Asp
NM_001382793.1:c.3195A>C	NP_001369722.1:p.Glu1065Asp
NM_001382794.1:c.3195A>C	NP_001369723.1:p.Glu1065Asp
NM_001382795.1:c.3189A>C	NP_001369724.1:p.Glu1063Asp
NM_001382796.1:c.3150A>C	NP_001369725.1:p.Glu1050Asp
NM_001382797.1:c.3138A>C	NP_001369726.1:p.Glu1046Asp
NM_001382798.1:c.3081A>C	NP_001369727.1:p.Glu1027Asp
NM_001382799.1:c.3057A>C	NP_001369728.1:p.Glu1019Asp
NM_001382800.1:c.3051A>C	NP_001369729.1:p.Glu1017Asp
NM_001382801.1:c.3033A>C	NP_001369730.1:p.Glu1011Asp
NM_001382802.1:c.2979A>C	NP_001369731.1:p.Glu993Asp
NM_001382803.1:c.3118-317A>C	NP_001369732.1:n.3118-317A>C
NM_001382804.1:c.2409A>C	NP_001369733.1:p.Glu803Asp
NM_001382805.1:c.2286A>C	NP_001369734.1:p.Glu762Asp
NM_001382806.1:c.2199A>C	NP_001369735.1:p.Glu733Asp
NM_004448.4:c.3237A>C MANE Select	NP_004439.2:p.Glu1079Asp
NR_110535.2:n.3475A>C