Canonical Allele Identifier: CA490314192

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534718C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242521C>T , CM000677.2:g.50242521C>T	GRCh38
NC_000015.9:g.50534718C>T , CM000677.1:g.50534718C>T	GRCh37
NC_000015.8:g.48322010C>T	NCBI36
NG_027487.1:g.28445G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1728G>A MANE Select	ENSP00000267845.3:p.Gln576=
ENST00000267845.7:c.1728G>A	ENSP00000267845.3:p.Gln576=
ENST00000543581.5:c.1629G>A	ENSP00000440252.1:p.Gln543=
ENST00000559816.1:n.1472G>A
NM_001306146.1:c.1629G>A	NP_001293075.1:p.Gln543=
NM_002112.3:c.1728G>A	NP_002103.2:p.Gln576=
XM_011521479.1:c.1491G>A	XP_011519781.1:p.Gln497=
XM_011521480.1:c.1296G>A	XP_011519782.1:p.Gln432=
XM_017022094.1:c.1833G>A	XP_016877583.1:p.Gln611=
XM_017022095.1:c.1734G>A	XP_016877584.1:p.Gln578=
XM_017022096.1:c.1605G>A	XP_016877585.1:p.Gln535=
XM_017022097.1:c.1596G>A	XP_016877586.1:p.Gln532=
XM_017022098.1:c.1401G>A	XP_016877587.1:p.Gln467=
NM_002112.4:c.1728G>A MANE Select	NP_002103.2:p.Gln576=
NM_001306146.2:c.1629G>A	NP_001293075.1:p.Gln543=