Canonical Allele Identifier: CA399303161

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849961
• MyVariant Identifiers: chr17:g.37881052T>A (hg19) ; chr17:g.39724799T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724799T>A , CM000679.2:g.39724799T>A	GRCh38
NC_000017.10:g.37881052T>A , CM000679.1:g.37881052T>A	GRCh37
NC_000017.9:g.35134578T>A	NCBI36
NG_007503.1:g.41660T>A , LRG_724:g.41660T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2381T>A MANE Select	ENSP00000269571.4:p.Val794Glu
ENST00000269571.9:c.2381T>A	ENSP00000269571.4:p.Val794Glu
ENST00000406381.6:c.2291T>A	ENSP00000385185.2:p.Val764Glu
ENST00000445658.6:c.1553T>A	ENSP00000404047.2:p.Val518Glu
ENST00000541774.5:c.2336T>A	ENSP00000446466.1:p.Val779Glu
ENST00000578373.5:c.*2171T>A	ENSP00000463427.1:n.*2171T>A
ENST00000580074.1:c.487T>A
ENST00000583038.5:n.3515T>A
ENST00000584450.5:c.2381T>A	ENSP00000463714.1:p.Val794Glu
ENST00000584601.5:c.2291T>A	ENSP00000462438.1:p.Val764Glu
NM_001005862.2:c.2291T>A , LRG_724t1:c.2291T>A	NP_001005862.1:p.Val764Glu
NM_001289936.1:c.2336T>A , LRG_724t4:c.2336T>A	NP_001276865.1:p.Val779Glu
NM_001289937.1:c.2381T>A	NP_001276866.1:p.Val794Glu
NM_004448.3:c.2381T>A , LRG_724t2:c.2381T>A	NP_004439.2:p.Val794Glu
NR_110535.1:n.2705T>A
XM_024450641.1:c.2519T>A	XP_024306409.1:p.Val840Glu
XM_024450642.1:c.2474T>A	XP_024306410.1:p.Val825Glu
XM_024450643.1:c.2429T>A	XP_024306411.1:p.Val810Glu
NM_001005862.3:c.2291T>A	NP_001005862.1:p.Val764Glu
NM_001289936.2:c.2336T>A	NP_001276865.1:p.Val779Glu
NM_001289937.2:c.2381T>A	NP_001276866.1:p.Val794Glu
NM_001382782.1:c.2291T>A	NP_001369711.1:p.Val764Glu
NM_001382783.1:c.2291T>A	NP_001369712.1:p.Val764Glu
NM_001382784.1:c.2498T>A	NP_001369713.1:p.Val833Glu
NM_001382785.1:c.2483T>A	NP_001369714.1:p.Val828Glu
NM_001382786.1:c.2462T>A	NP_001369715.1:p.Val821Glu
NM_001382787.1:c.2456T>A	NP_001369716.1:p.Val819Glu
NM_001382788.1:c.2411T>A	NP_001369717.1:p.Val804Glu
NM_001382789.1:c.2402T>A	NP_001369718.1:p.Val801Glu
NM_001382790.1:c.2378T>A	NP_001369719.1:p.Val793Glu
NM_001382791.1:c.2372T>A	NP_001369720.1:p.Val791Glu
NM_001382792.1:c.2345T>A	NP_001369721.1:p.Val782Glu
NM_001382793.1:c.2339T>A	NP_001369722.1:p.Val780Glu
NM_001382794.1:c.2339T>A	NP_001369723.1:p.Val780Glu
NM_001382795.1:c.2333T>A	NP_001369724.1:p.Val778Glu
NM_001382796.1:c.2381T>A	NP_001369725.1:p.Val794Glu
NM_001382797.1:c.2282T>A	NP_001369726.1:p.Val761Glu
NM_001382798.1:c.2381T>A	NP_001369727.1:p.Val794Glu
NM_001382799.1:c.2201T>A	NP_001369728.1:p.Val734Glu
NM_001382800.1:c.2308-250T>A	NP_001369729.1:n.2308-250T>A
NM_001382801.1:c.2333T>A	NP_001369730.1:p.Val778Glu
NM_001382802.1:c.2123T>A	NP_001369731.1:p.Val708Glu
NM_001382803.1:c.2339T>A	NP_001369732.1:p.Val780Glu
NM_001382804.1:c.1553T>A	NP_001369733.1:p.Val518Glu
NM_001382805.1:c.2208+1139T>A	NP_001369734.1:n.2208+1139T>A
NM_001382806.1:c.1343T>A	NP_001369735.1:p.Val448Glu
NM_004448.4:c.2381T>A MANE Select	NP_004439.2:p.Val794Glu
NR_110535.2:n.2619T>A