Canonical Allele Identifier: CA2176326565

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242367T= , CM000677.2:g.50242367T=	GRCh38
NC_000015.9:g.50534564T= , CM000677.1:g.50534564T=	GRCh37
NC_000015.8:g.48321856T=	NCBI36
NG_027487.1:g.28599A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1882A= MANE Select	ENSP00000267845.3:p.Ser628=
ENST00000267845.7:c.1882A=	ENSP00000267845.3:p.Ser628=
ENST00000543581.5:c.1783A=	ENSP00000440252.1:p.Ser595=
ENST00000559816.1:n.1626A=
NM_001306146.1:c.1783A=	NP_001293075.1:p.Ser595=
NM_002112.3:c.1882A=	NP_002103.2:p.Ser628=
XM_011521479.1:c.1645A=	XP_011519781.1:p.Ser549=
XM_011521480.1:c.1450A=	XP_011519782.1:p.Ser484=
XM_017022094.1:c.1987A=	XP_016877583.1:p.Ser663=
XM_017022095.1:c.1888A=	XP_016877584.1:p.Ser630=
XM_017022096.1:c.1759A=	XP_016877585.1:p.Ser587=
XM_017022097.1:c.1750A=	XP_016877586.1:p.Ser584=
XM_017022098.1:c.1555A=	XP_016877587.1:p.Ser519=
NM_002112.4:c.1882A= MANE Select	NP_002103.2:p.Ser628=
NM_001306146.2:c.1783A=	NP_001293075.1:p.Ser595=