Canonical Allele Identifier: CA2176326615

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242497G= , CM000677.2:g.50242497G=	GRCh38
NC_000015.9:g.50534694G= , CM000677.1:g.50534694G=	GRCh37
NC_000015.8:g.48321986G=	NCBI36
NG_027487.1:g.28469C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1752C= MANE Select	ENSP00000267845.3:p.Ser584=
ENST00000267845.7:c.1752C=	ENSP00000267845.3:p.Ser584=
ENST00000543581.5:c.1653C=	ENSP00000440252.1:p.Ser551=
ENST00000559816.1:n.1496C=
NM_001306146.1:c.1653C=	NP_001293075.1:p.Ser551=
NM_002112.3:c.1752C=	NP_002103.2:p.Ser584=
XM_011521479.1:c.1515C=	XP_011519781.1:p.Ser505=
XM_011521480.1:c.1320C=	XP_011519782.1:p.Ser440=
XM_017022094.1:c.1857C=	XP_016877583.1:p.Ser619=
XM_017022095.1:c.1758C=	XP_016877584.1:p.Ser586=
XM_017022096.1:c.1629C=	XP_016877585.1:p.Ser543=
XM_017022097.1:c.1620C=	XP_016877586.1:p.Ser540=
XM_017022098.1:c.1425C=	XP_016877587.1:p.Ser475=
NM_002112.4:c.1752C= MANE Select	NP_002103.2:p.Ser584=
NM_001306146.2:c.1653C=	NP_001293075.1:p.Ser551=