Canonical Allele Identifier: CA354076762

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120365191T>G (hg19) ; chr3:g.120646344T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646344T>G , CM000665.2:g.120646344T>G	GRCh38
NC_000003.11:g.120365191T>G , CM000665.1:g.120365191T>G	GRCh37
NC_000003.10:g.121847881T>G	NCBI36
NG_011957.1:g.41138A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.572A>C MANE Select	ENSP00000283871.5:p.Asp191Ala
ENST00000283871.9:c.572A>C	ENSP00000283871.5:p.Asp191Ala
ENST00000475447.2:c.103A>C
ENST00000492108.5:c.180+629A>C	ENSP00000419838.1:n.180+629A>C
NM_000187.3:c.572A>C	NP_000178.2:p.Asp191Ala
XM_005247412.1:c.549+629A>C	XP_005247469.1:n.549+629A>C
XM_005247413.1:c.572A>C	XP_005247470.1:p.Asp191Ala
XM_005247414.3:c.572A>C	XP_005247471.1:p.Asp191Ala
XM_011512746.1:c.572A>C	XP_011511048.1:p.Asp191Ala
XM_005247412.2:c.549+629A>C	XP_005247469.1:n.549+629A>C
XM_005247413.2:c.572A>C	XP_005247470.1:p.Asp191Ala
XM_005247414.5:c.572A>C	XP_005247471.1:p.Asp191Ala
XM_011512746.2:c.572A>C	XP_011511048.1:p.Asp191Ala
XM_017006277.2:c.149A>C	XP_016861766.1:p.Asp50Ala
NM_000187.4:c.572A>C MANE Select	NP_000178.2:p.Asp191Ala