Canonical Allele Identifier: CA2176326612

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242484T= , CM000677.2:g.50242484T=	GRCh38
NC_000015.9:g.50534681T= , CM000677.1:g.50534681T=	GRCh37
NC_000015.8:g.48321973T=	NCBI36
NG_027487.1:g.28482A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1765A= MANE Select	ENSP00000267845.3:p.Ser589=
ENST00000267845.7:c.1765A=	ENSP00000267845.3:p.Ser589=
ENST00000543581.5:c.1666A=	ENSP00000440252.1:p.Ser556=
ENST00000559816.1:n.1509A=
NM_001306146.1:c.1666A=	NP_001293075.1:p.Ser556=
NM_002112.3:c.1765A=	NP_002103.2:p.Ser589=
XM_011521479.1:c.1528A=	XP_011519781.1:p.Ser510=
XM_011521480.1:c.1333A=	XP_011519782.1:p.Ser445=
XM_017022094.1:c.1870A=	XP_016877583.1:p.Ser624=
XM_017022095.1:c.1771A=	XP_016877584.1:p.Ser591=
XM_017022096.1:c.1642A=	XP_016877585.1:p.Ser548=
XM_017022097.1:c.1633A=	XP_016877586.1:p.Ser545=
XM_017022098.1:c.1438A=	XP_016877587.1:p.Ser480=
NM_002112.4:c.1765A= MANE Select	NP_002103.2:p.Ser589=
NM_001306146.2:c.1666A=	NP_001293075.1:p.Ser556=