Canonical Allele Identifier: CA2176301277

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50252520C= , CM000677.2:g.50252520C=	GRCh38
NC_000015.9:g.50544717C= , CM000677.1:g.50544717C=	GRCh37
NC_000015.8:g.48332009C=	NCBI36
NG_027487.1:g.18446G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002112.4:c.951G= MANE Select	NP_002103.2:p.Trp317=
ENST00000267845.8:c.951G= MANE Select	ENSP00000267845.3:p.Trp317=
NM_001306146.1:c.951G=	NP_001293075.1:p.Trp317=
NM_001306146.2:c.951G=	NP_001293075.1:p.Trp317=
NM_002112.3:c.951G=	NP_002103.2:p.Trp317=
ENST00000267845.7:c.951G=	ENSP00000267845.3:p.Trp317=
ENST00000543581.5:c.951G=	ENSP00000440252.1:p.Trp317=
ENST00000559816.1:n.695G=
XM_011521479.1:c.714G=	XP_011519781.1:p.Trp238=
XM_011521480.1:c.519G=	XP_011519782.1:p.Trp173=
XM_011521481.1:c.951G=	XP_011519783.1:p.Trp317=
XM_017022094.1:c.1056G=	XP_016877583.1:p.Trp352=
XM_017022095.1:c.1056G=	XP_016877584.1:p.Trp352=
XM_017022096.1:c.828G=	XP_016877585.1:p.Trp276=
XM_017022097.1:c.819G=	XP_016877586.1:p.Trp273=
XM_017022098.1:c.624G=	XP_016877587.1:p.Trp208=
XM_017022099.1:c.1056G=	XP_016877588.1:p.Trp352=