Canonical Allele Identifier: CA399479130

Gene: HAP1

Linked Data

• MyVariant Identifiers: chr17:g.39883395T>A (hg19) ; chr17:g.41727143T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41727143T>A , CM000679.2:g.41727143T>A	GRCh38
NC_000017.10:g.39883395T>A , CM000679.1:g.39883395T>A	GRCh37
NC_000017.9:g.37136921T>A	NCBI36
NG_009090.2:g.64570A>T , LRG_401:g.64570A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347901.9:c.1277A>T MANE Select	ENSP00000334002.4:p.Glu426Val
ENST00000310778.5:c.1433A>T	ENSP00000309392.5:p.Glu478Val
ENST00000341193.9:c.1226A>T	ENSP00000343170.5:p.Glu409Val
ENST00000347901.8:c.1277A>T	ENSP00000334002.4:p.Glu426Val
ENST00000393939.6:c.1202A>T	ENSP00000377513.2:p.Glu401Val
NM_001079870.1:c.1226A>T	NP_001073339.1:p.Glu409Val
NM_001079871.1:c.1202A>T	NP_001073340.1:p.Glu401Val
NM_177977.2:c.1277A>T	NP_817084.2:p.Glu426Val
NM_001367459.1:c.1373A>T	NP_001354388.1:p.Glu458Val
NM_001367460.1:c.1337A>T	NP_001354389.1:p.Glu446Val
NM_001367461.1:c.1202A>T	NP_001354390.1:p.Glu401Val
NM_001367462.1:c.1202A>T	NP_001354391.1:p.Glu401Val
NM_177977.3:c.1277A>T MANE Select	NP_817084.2:p.Glu426Val