Canonical Allele Identifier: CA2176326587

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242421A= , CM000677.2:g.50242421A=	GRCh38
NC_000015.9:g.50534618A= , CM000677.1:g.50534618A=	GRCh37
NC_000015.8:g.48321910A=	NCBI36
NG_027487.1:g.28545T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1828T= MANE Select	ENSP00000267845.3:p.Ser610=
ENST00000267845.7:c.1828T=	ENSP00000267845.3:p.Ser610=
ENST00000543581.5:c.1729T=	ENSP00000440252.1:p.Ser577=
ENST00000559816.1:n.1572T=
NM_001306146.1:c.1729T=	NP_001293075.1:p.Ser577=
NM_002112.3:c.1828T=	NP_002103.2:p.Ser610=
XM_011521479.1:c.1591T=	XP_011519781.1:p.Ser531=
XM_011521480.1:c.1396T=	XP_011519782.1:p.Ser466=
XM_017022094.1:c.1933T=	XP_016877583.1:p.Ser645=
XM_017022095.1:c.1834T=	XP_016877584.1:p.Ser612=
XM_017022096.1:c.1705T=	XP_016877585.1:p.Ser569=
XM_017022097.1:c.1696T=	XP_016877586.1:p.Ser566=
XM_017022098.1:c.1501T=	XP_016877587.1:p.Ser501=
NM_002112.4:c.1828T= MANE Select	NP_002103.2:p.Ser610=
NM_001306146.2:c.1729T=	NP_001293075.1:p.Ser577=