Canonical Allele Identifier: CA1397090711

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120633181T= , CM000665.2:g.120633181T=	GRCh38
NC_000003.11:g.120352028T= , CM000665.1:g.120352028T=	GRCh37
NC_000003.10:g.121834718T=	NCBI36
NG_011957.1:g.54301A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.1154A= MANE Select	ENSP00000283871.5:p.Lys385=
ENST00000283871.9:c.1154A=	ENSP00000283871.5:p.Lys385=
ENST00000470321.1:n.494A=
ENST00000492108.5:c.433A=	ENSP00000419838.1:n.433A=
NM_000187.3:c.1154A=	NP_000178.2:p.Lys385=
XM_005247412.1:c.929A=	XP_005247469.1:p.Lys310=
XM_005247412.2:c.929A=	XP_005247469.1:p.Lys310=
XM_017006277.2:c.731A=	XP_016861766.1:p.Lys244=
NM_000187.4:c.1154A= MANE Select	NP_000178.2:p.Lys385=