Canonical Allele Identifier: CA2176307714

Gene: HDC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50259733C= , CM000677.2:g.50259733C=	GRCh38
NC_000015.9:g.50551930C= , CM000677.1:g.50551930C=	GRCh37
NC_000015.8:g.48339222C=	NCBI36
NG_027487.1:g.11233G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002112.4:c.205-1216G= MANE Select	NP_002103.2:n.205-1216G=
ENST00000267845.8:c.205-1216G= MANE Select	ENSP00000267845.3:n.205-1216G=
NM_001306146.1:c.205-1216G=	NP_001293075.1:n.205-1216G=
NM_001306146.2:c.205-1216G=	NP_001293075.1:n.205-1216G=
NM_002112.3:c.205-1216G=	NP_002103.2:n.205-1216G=
ENST00000267845.7:c.205-1216G=	ENSP00000267845.3:n.205-1216G=
ENST00000543581.5:c.205-1216G=	ENSP00000440252.1:n.205-1216G=
ENST00000558679.1:n.547-1216G=
ENST00000558761.5:n.307+3502G=
ENST00000559190.5:n.82-1216G=
ENST00000559683.1:c.187-1216G=	ENSP00000453183.1:n.187-1216G=
XM_011521479.1:c.204+3502G=	XP_011519781.1:n.204+3502G=
XM_011521481.1:c.205-1216G=	XP_011519783.1:n.205-1216G=
XM_017022094.1:c.205-1216G=	XP_016877583.1:n.205-1216G=
XM_017022095.1:c.205-1216G=	XP_016877584.1:n.205-1216G=
XM_017022097.1:c.204+3502G=	XP_016877586.1:n.204+3502G=
XM_017022099.1:c.205-1216G=	XP_016877588.1:n.205-1216G=