Canonical Allele Identifier: CA490314038

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534625C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242428C>A , CM000677.2:g.50242428C>A	GRCh38
NC_000015.9:g.50534625C>A , CM000677.1:g.50534625C>A	GRCh37
NC_000015.8:g.48321917C>A	NCBI36
NG_027487.1:g.28538G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1821G>T MANE Select	ENSP00000267845.3:p.Gly607=
ENST00000267845.7:c.1821G>T	ENSP00000267845.3:p.Gly607=
ENST00000543581.5:c.1722G>T	ENSP00000440252.1:p.Gly574=
ENST00000559816.1:n.1565G>T
NM_001306146.1:c.1722G>T	NP_001293075.1:p.Gly574=
NM_002112.3:c.1821G>T	NP_002103.2:p.Gly607=
XM_011521479.1:c.1584G>T	XP_011519781.1:p.Gly528=
XM_011521480.1:c.1389G>T	XP_011519782.1:p.Gly463=
XM_017022094.1:c.1926G>T	XP_016877583.1:p.Gly642=
XM_017022095.1:c.1827G>T	XP_016877584.1:p.Gly609=
XM_017022096.1:c.1698G>T	XP_016877585.1:p.Gly566=
XM_017022097.1:c.1689G>T	XP_016877586.1:p.Gly563=
XM_017022098.1:c.1494G>T	XP_016877587.1:p.Gly498=
NM_002112.4:c.1821G>T MANE Select	NP_002103.2:p.Gly607=
NM_001306146.2:c.1722G>T	NP_001293075.1:p.Gly574=