Canonical Allele Identifier: CA490314137

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534685G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242488G>A , CM000677.2:g.50242488G>A	GRCh38
NC_000015.9:g.50534685G>A , CM000677.1:g.50534685G>A	GRCh37
NC_000015.8:g.48321977G>A	NCBI36
NG_027487.1:g.28478C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1761C>T MANE Select	ENSP00000267845.3:p.Cys587=
ENST00000267845.7:c.1761C>T	ENSP00000267845.3:p.Cys587=
ENST00000543581.5:c.1662C>T	ENSP00000440252.1:p.Cys554=
ENST00000559816.1:n.1505C>T
NM_001306146.1:c.1662C>T	NP_001293075.1:p.Cys554=
NM_002112.3:c.1761C>T	NP_002103.2:p.Cys587=
XM_011521479.1:c.1524C>T	XP_011519781.1:p.Cys508=
XM_011521480.1:c.1329C>T	XP_011519782.1:p.Cys443=
XM_017022094.1:c.1866C>T	XP_016877583.1:p.Cys622=
XM_017022095.1:c.1767C>T	XP_016877584.1:p.Cys589=
XM_017022096.1:c.1638C>T	XP_016877585.1:p.Cys546=
XM_017022097.1:c.1629C>T	XP_016877586.1:p.Cys543=
XM_017022098.1:c.1434C>T	XP_016877587.1:p.Cys478=
NM_002112.4:c.1761C>T MANE Select	NP_002103.2:p.Cys587=
NM_001306146.2:c.1662C>T	NP_001293075.1:p.Cys554=