Canonical Allele Identifier: CA399302774

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37880980A>T (hg19) ; chr17:g.39724727A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724727A>T , CM000679.2:g.39724727A>T	GRCh38
NC_000017.10:g.37880980A>T , CM000679.1:g.37880980A>T	GRCh37
NC_000017.9:g.35134506A>T	NCBI36
NG_007503.1:g.41588A>T , LRG_724:g.41588A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2309A>T MANE Select	ENSP00000269571.4:p.Glu770Val
ENST00000269571.9:c.2309A>T	ENSP00000269571.4:p.Glu770Val
ENST00000406381.6:c.2219A>T	ENSP00000385185.2:p.Glu740Val
ENST00000445658.6:c.1481A>T	ENSP00000404047.2:p.Glu494Val
ENST00000541774.5:c.2264A>T	ENSP00000446466.1:p.Glu755Val
ENST00000578373.5:c.*2099A>T	ENSP00000463427.1:n.*2099A>T
ENST00000580074.1:c.415A>T
ENST00000583038.5:n.3443A>T
ENST00000584450.5:c.2309A>T	ENSP00000463714.1:p.Glu770Val
ENST00000584601.5:c.2219A>T	ENSP00000462438.1:p.Glu740Val
NM_001005862.2:c.2219A>T , LRG_724t1:c.2219A>T	NP_001005862.1:p.Glu740Val
NM_001289936.1:c.2264A>T , LRG_724t4:c.2264A>T	NP_001276865.1:p.Glu755Val
NM_001289937.1:c.2309A>T	NP_001276866.1:p.Glu770Val
NM_004448.3:c.2309A>T , LRG_724t2:c.2309A>T	NP_004439.2:p.Glu770Val
NR_110535.1:n.2633A>T
XM_024450641.1:c.2447A>T	XP_024306409.1:p.Glu816Val
XM_024450642.1:c.2402A>T	XP_024306410.1:p.Glu801Val
XM_024450643.1:c.2357A>T	XP_024306411.1:p.Glu786Val
NM_001005862.3:c.2219A>T	NP_001005862.1:p.Glu740Val
NM_001289936.2:c.2264A>T	NP_001276865.1:p.Glu755Val
NM_001289937.2:c.2309A>T	NP_001276866.1:p.Glu770Val
NM_001382782.1:c.2219A>T	NP_001369711.1:p.Glu740Val
NM_001382783.1:c.2219A>T	NP_001369712.1:p.Glu740Val
NM_001382784.1:c.2426A>T	NP_001369713.1:p.Glu809Val
NM_001382785.1:c.2411A>T	NP_001369714.1:p.Glu804Val
NM_001382786.1:c.2390A>T	NP_001369715.1:p.Glu797Val
NM_001382787.1:c.2384A>T	NP_001369716.1:p.Glu795Val
NM_001382788.1:c.2339A>T	NP_001369717.1:p.Glu780Val
NM_001382789.1:c.2330A>T	NP_001369718.1:p.Glu777Val
NM_001382790.1:c.2306A>T	NP_001369719.1:p.Glu769Val
NM_001382791.1:c.2300A>T	NP_001369720.1:p.Glu767Val
NM_001382792.1:c.2273A>T	NP_001369721.1:p.Glu758Val
NM_001382793.1:c.2267A>T	NP_001369722.1:p.Glu756Val
NM_001382794.1:c.2267A>T	NP_001369723.1:p.Glu756Val
NM_001382795.1:c.2261A>T	NP_001369724.1:p.Glu754Val
NM_001382796.1:c.2309A>T	NP_001369725.1:p.Glu770Val
NM_001382797.1:c.2210A>T	NP_001369726.1:p.Glu737Val
NM_001382798.1:c.2309A>T	NP_001369727.1:p.Glu770Val
NM_001382799.1:c.2129A>T	NP_001369728.1:p.Glu710Val
NM_001382800.1:c.2308-322A>T	NP_001369729.1:n.2308-322A>T
NM_001382801.1:c.2261A>T	NP_001369730.1:p.Glu754Val
NM_001382802.1:c.2051A>T	NP_001369731.1:p.Glu684Val
NM_001382803.1:c.2267A>T	NP_001369732.1:p.Glu756Val
NM_001382804.1:c.1481A>T	NP_001369733.1:p.Glu494Val
NM_001382805.1:c.2208+1067A>T	NP_001369734.1:n.2208+1067A>T
NM_001382806.1:c.1271A>T	NP_001369735.1:p.Glu424Val
NM_004448.4:c.2309A>T MANE Select	NP_004439.2:p.Glu770Val
NR_110535.2:n.2547A>T