Canonical Allele Identifier: CA490314165

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534700C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242503C>A , CM000677.2:g.50242503C>A	GRCh38
NC_000015.9:g.50534700C>A , CM000677.1:g.50534700C>A	GRCh37
NC_000015.8:g.48321992C>A	NCBI36
NG_027487.1:g.28463G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1746G>T MANE Select	ENSP00000267845.3:p.Val582=
ENST00000267845.7:c.1746G>T	ENSP00000267845.3:p.Val582=
ENST00000543581.5:c.1647G>T	ENSP00000440252.1:p.Val549=
ENST00000559816.1:n.1490G>T
NM_001306146.1:c.1647G>T	NP_001293075.1:p.Val549=
NM_002112.3:c.1746G>T	NP_002103.2:p.Val582=
XM_011521479.1:c.1509G>T	XP_011519781.1:p.Val503=
XM_011521480.1:c.1314G>T	XP_011519782.1:p.Val438=
XM_017022094.1:c.1851G>T	XP_016877583.1:p.Val617=
XM_017022095.1:c.1752G>T	XP_016877584.1:p.Val584=
XM_017022096.1:c.1623G>T	XP_016877585.1:p.Val541=
XM_017022097.1:c.1614G>T	XP_016877586.1:p.Val538=
XM_017022098.1:c.1419G>T	XP_016877587.1:p.Val473=
NM_002112.4:c.1746G>T MANE Select	NP_002103.2:p.Val582=
NM_001306146.2:c.1647G>T	NP_001293075.1:p.Val549=