Canonical Allele Identifier: CA490314183

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534712C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242515C>T , CM000677.2:g.50242515C>T	GRCh38
NC_000015.9:g.50534712C>T , CM000677.1:g.50534712C>T	GRCh37
NC_000015.8:g.48322004C>T	NCBI36
NG_027487.1:g.28451G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1734G>A MANE Select	ENSP00000267845.3:p.Lys578=
ENST00000267845.7:c.1734G>A	ENSP00000267845.3:p.Lys578=
ENST00000543581.5:c.1635G>A	ENSP00000440252.1:p.Lys545=
ENST00000559816.1:n.1478G>A
NM_001306146.1:c.1635G>A	NP_001293075.1:p.Lys545=
NM_002112.3:c.1734G>A	NP_002103.2:p.Lys578=
XM_011521479.1:c.1497G>A	XP_011519781.1:p.Lys499=
XM_011521480.1:c.1302G>A	XP_011519782.1:p.Lys434=
XM_017022094.1:c.1839G>A	XP_016877583.1:p.Lys613=
XM_017022095.1:c.1740G>A	XP_016877584.1:p.Lys580=
XM_017022096.1:c.1611G>A	XP_016877585.1:p.Lys537=
XM_017022097.1:c.1602G>A	XP_016877586.1:p.Lys534=
XM_017022098.1:c.1407G>A	XP_016877587.1:p.Lys469=
NM_002112.4:c.1734G>A MANE Select	NP_002103.2:p.Lys578=
NM_001306146.2:c.1635G>A	NP_001293075.1:p.Lys545=