Canonical Allele Identifier: CA399479053

Gene: HAP1

Linked Data

• MyVariant Identifiers: chr17:g.39883384C>G (hg19) ; chr17:g.41727132C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41727132C>G , CM000679.2:g.41727132C>G	GRCh38
NC_000017.10:g.39883384C>G , CM000679.1:g.39883384C>G	GRCh37
NC_000017.9:g.37136910C>G	NCBI36
NG_009090.2:g.64581G>C , LRG_401:g.64581G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347901.9:c.1288G>C MANE Select	ENSP00000334002.4:p.Gly430Arg
ENST00000310778.5:c.1444G>C	ENSP00000309392.5:p.Gly482Arg
ENST00000341193.9:c.1237G>C	ENSP00000343170.5:p.Gly413Arg
ENST00000347901.8:c.1288G>C	ENSP00000334002.4:p.Gly430Arg
ENST00000393939.6:c.1213G>C	ENSP00000377513.2:p.Gly405Arg
NM_001079870.1:c.1237G>C	NP_001073339.1:p.Gly413Arg
NM_001079871.1:c.1213G>C	NP_001073340.1:p.Gly405Arg
NM_177977.2:c.1288G>C	NP_817084.2:p.Gly430Arg
NM_001367459.1:c.1384G>C	NP_001354388.1:p.Gly462Arg
NM_001367460.1:c.1348G>C	NP_001354389.1:p.Gly450Arg
NM_001367461.1:c.1213G>C	NP_001354390.1:p.Gly405Arg
NM_001367462.1:c.1213G>C	NP_001354391.1:p.Gly405Arg
NM_177977.3:c.1288G>C MANE Select	NP_817084.2:p.Gly430Arg