Canonical Allele Identifier: CA2176326625

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242517T= , CM000677.2:g.50242517T=	GRCh38
NC_000015.9:g.50534714T= , CM000677.1:g.50534714T=	GRCh37
NC_000015.8:g.48322006T=	NCBI36
NG_027487.1:g.28449A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1732A= MANE Select	ENSP00000267845.3:p.Lys578=
ENST00000267845.7:c.1732A=	ENSP00000267845.3:p.Lys578=
ENST00000543581.5:c.1633A=	ENSP00000440252.1:p.Lys545=
ENST00000559816.1:n.1476A=
NM_001306146.1:c.1633A=	NP_001293075.1:p.Lys545=
NM_002112.3:c.1732A=	NP_002103.2:p.Lys578=
XM_011521479.1:c.1495A=	XP_011519781.1:p.Lys499=
XM_011521480.1:c.1300A=	XP_011519782.1:p.Lys434=
XM_017022094.1:c.1837A=	XP_016877583.1:p.Lys613=
XM_017022095.1:c.1738A=	XP_016877584.1:p.Lys580=
XM_017022096.1:c.1609A=	XP_016877585.1:p.Lys537=
XM_017022097.1:c.1600A=	XP_016877586.1:p.Lys534=
XM_017022098.1:c.1405A=	XP_016877587.1:p.Lys469=
NM_002112.4:c.1732A= MANE Select	NP_002103.2:p.Lys578=
NM_001306146.2:c.1633A=	NP_001293075.1:p.Lys545=