Canonical Allele Identifier: CA1397096525

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646229T= , CM000665.2:g.120646229T=	GRCh38
NC_000003.11:g.120365076T= , CM000665.1:g.120365076T=	GRCh37
NC_000003.10:g.121847766T=	NCBI36
NG_011957.1:g.41253A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.649+38A= MANE Select	ENSP00000283871.5:n.649+38A=
ENST00000283871.9:c.649+38A=	ENSP00000283871.5:n.649+38A=
ENST00000475447.2:c.180+38A=
ENST00000492108.5:c.180+744A=	ENSP00000419838.1:n.180+744A=
ENST00000494453.1:c.69+38A=
NM_000187.3:c.649+38A=	NP_000178.2:n.649+38A=
XM_005247412.1:c.549+744A=	XP_005247469.1:n.549+744A=
XM_005247413.1:c.649+38A=	XP_005247470.1:n.649+38A=
XM_005247414.3:c.649+38A=	XP_005247471.1:n.649+38A=
XM_011512746.1:c.649+38A=	XP_011511048.1:n.649+38A=
XM_005247412.2:c.549+744A=	XP_005247469.1:n.549+744A=
XM_005247413.2:c.649+38A=	XP_005247470.1:n.649+38A=
XM_005247414.5:c.649+38A=	XP_005247471.1:n.649+38A=
XM_011512746.2:c.649+38A=	XP_011511048.1:n.649+38A=
XM_017006277.2:c.226+38A=	XP_016861766.1:n.226+38A=
NM_000187.4:c.649+38A= MANE Select	NP_000178.2:n.649+38A=