Canonical Allele Identifier: CA399304072

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145861999
• MyVariant Identifiers: chr17:g.37881303G>T (hg19) ; chr17:g.39725050G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725050G>T , CM000679.2:g.39725050G>T	GRCh38
NC_000017.10:g.37881303G>T , CM000679.1:g.37881303G>T	GRCh37
NC_000017.9:g.35134829G>T	NCBI36
NG_007503.1:g.41911G>T , LRG_724:g.41911G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2495G>T MANE Select	ENSP00000269571.4:p.Gly832Val
ENST00000269571.9:c.2495G>T	ENSP00000269571.4:p.Gly832Val
ENST00000406381.6:c.2405G>T	ENSP00000385185.2:p.Gly802Val
ENST00000445658.6:c.1667G>T	ENSP00000404047.2:p.Gly556Val
ENST00000541774.5:c.2450G>T	ENSP00000446466.1:p.Gly817Val
ENST00000578373.5:c.*2285G>T	ENSP00000463427.1:n.*2285G>T
ENST00000580074.1:c.601G>T
ENST00000583038.5:n.3629G>T
ENST00000584450.5:c.2495G>T	ENSP00000463714.1:p.Gly832Val
ENST00000584601.5:c.2405G>T	ENSP00000462438.1:p.Gly802Val
NM_001005862.2:c.2405G>T , LRG_724t1:c.2405G>T	NP_001005862.1:p.Gly802Val
NM_001289936.1:c.2450G>T , LRG_724t4:c.2450G>T	NP_001276865.1:p.Gly817Val
NM_001289937.1:c.2495G>T	NP_001276866.1:p.Gly832Val
NM_004448.3:c.2495G>T , LRG_724t2:c.2495G>T	NP_004439.2:p.Gly832Val
NR_110535.1:n.2819G>T
XM_024450641.1:c.2633G>T	XP_024306409.1:p.Gly878Val
XM_024450642.1:c.2588G>T	XP_024306410.1:p.Gly863Val
XM_024450643.1:c.2543G>T	XP_024306411.1:p.Gly848Val
NM_001005862.3:c.2405G>T	NP_001005862.1:p.Gly802Val
NM_001289936.2:c.2450G>T	NP_001276865.1:p.Gly817Val
NM_001289937.2:c.2495G>T	NP_001276866.1:p.Gly832Val
NM_001382782.1:c.2405G>T	NP_001369711.1:p.Gly802Val
NM_001382783.1:c.2405G>T	NP_001369712.1:p.Gly802Val
NM_001382784.1:c.2612G>T	NP_001369713.1:p.Gly871Val
NM_001382785.1:c.2597G>T	NP_001369714.1:p.Gly866Val
NM_001382786.1:c.2576G>T	NP_001369715.1:p.Gly859Val
NM_001382787.1:c.2570G>T	NP_001369716.1:p.Gly857Val
NM_001382788.1:c.2525G>T	NP_001369717.1:p.Gly842Val
NM_001382789.1:c.2516G>T	NP_001369718.1:p.Gly839Val
NM_001382790.1:c.2492G>T	NP_001369719.1:p.Gly831Val
NM_001382791.1:c.2486G>T	NP_001369720.1:p.Gly829Val
NM_001382792.1:c.2459G>T	NP_001369721.1:p.Gly820Val
NM_001382793.1:c.2453G>T	NP_001369722.1:p.Gly818Val
NM_001382794.1:c.2453G>T	NP_001369723.1:p.Gly818Val
NM_001382795.1:c.2447G>T	NP_001369724.1:p.Gly816Val
NM_001382796.1:c.2495G>T	NP_001369725.1:p.Gly832Val
NM_001382797.1:c.2396G>T	NP_001369726.1:p.Gly799Val
NM_001382798.1:c.2493+139G>T	NP_001369727.1:n.2493+139G>T
NM_001382799.1:c.2315G>T	NP_001369728.1:p.Gly772Val
NM_001382800.1:c.2309G>T	NP_001369729.1:p.Gly770Val
NM_001382801.1:c.2445+139G>T	NP_001369730.1:n.2445+139G>T
NM_001382802.1:c.2237G>T	NP_001369731.1:p.Gly746Val
NM_001382803.1:c.2453G>T	NP_001369732.1:p.Gly818Val
NM_001382804.1:c.1667G>T	NP_001369733.1:p.Gly556Val
NM_001382805.1:c.2208+1390G>T	NP_001369734.1:n.2208+1390G>T
NM_001382806.1:c.1457G>T	NP_001369735.1:p.Gly486Val
NM_004448.4:c.2495G>T MANE Select	NP_004439.2:p.Gly832Val
NR_110535.2:n.2733G>T