Canonical Allele Identifier: CA500010389

Gene: HAP1

Linked Data

• MyVariant Identifiers: chr17:g.39883354T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41727102T>G , CM000679.2:g.41727102T>G	GRCh38
NC_000017.10:g.39883354T>G , CM000679.1:g.39883354T>G	GRCh37
NC_000017.9:g.37136880T>G	NCBI36
NG_009090.2:g.64611A>C , LRG_401:g.64611A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347901.9:c.1318A>C MANE Select	ENSP00000334002.4:p.Arg440=
ENST00000310778.5:c.1474A>C	ENSP00000309392.5:p.Arg492=
ENST00000341193.9:c.1267A>C	ENSP00000343170.5:p.Arg423=
ENST00000347901.8:c.1318A>C	ENSP00000334002.4:p.Arg440=
ENST00000393939.6:c.1243A>C	ENSP00000377513.2:p.Arg415=
NM_001079870.1:c.1267A>C	NP_001073339.1:p.Arg423=
NM_001079871.1:c.1243A>C	NP_001073340.1:p.Arg415=
NM_177977.2:c.1318A>C	NP_817084.2:p.Arg440=
NM_001367459.1:c.1414A>C	NP_001354388.1:p.Arg472=
NM_001367460.1:c.1378A>C	NP_001354389.1:p.Arg460=
NM_001367461.1:c.1243A>C	NP_001354390.1:p.Arg415=
NM_001367462.1:c.1243A>C	NP_001354391.1:p.Arg415=
NM_177977.3:c.1318A>C MANE Select	NP_817084.2:p.Arg440=