Canonical Allele Identifier: CA2176326550

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242326G= , CM000677.2:g.50242326G=	GRCh38
NC_000015.9:g.50534523G= , CM000677.1:g.50534523G=	GRCh37
NC_000015.8:g.48321815G=	NCBI36
NG_027487.1:g.28640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1923C= MANE Select	ENSP00000267845.3:p.Ser641=
ENST00000267845.7:c.1923C=	ENSP00000267845.3:p.Ser641=
ENST00000543581.5:c.1824C=	ENSP00000440252.1:p.Ser608=
ENST00000559816.1:n.1667C=
NM_001306146.1:c.1824C=	NP_001293075.1:p.Ser608=
NM_002112.3:c.1923C=	NP_002103.2:p.Ser641=
XM_011521479.1:c.1686C=	XP_011519781.1:p.Ser562=
XM_011521480.1:c.1491C=	XP_011519782.1:p.Ser497=
XM_017022094.1:c.2028C=	XP_016877583.1:p.Ser676=
XM_017022095.1:c.1929C=	XP_016877584.1:p.Ser643=
XM_017022096.1:c.1800C=	XP_016877585.1:p.Ser600=
XM_017022097.1:c.1791C=	XP_016877586.1:p.Ser597=
XM_017022098.1:c.1596C=	XP_016877587.1:p.Ser532=
NM_002112.4:c.1923C= MANE Select	NP_002103.2:p.Ser641=
NM_001306146.2:c.1824C=	NP_001293075.1:p.Ser608=