Canonical Allele Identifier: CA354081075

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120389290T>G (hg19) ; chr3:g.120670443T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120670443T>G , CM000665.2:g.120670443T>G	GRCh38
NC_000003.11:g.120389290T>G , CM000665.1:g.120389290T>G	GRCh37
NC_000003.10:g.121871980T>G	NCBI36
NG_011957.1:g.17039A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.266A>C MANE Select	ENSP00000283871.5:p.Asp89Ala
ENST00000283871.9:c.266A>C	ENSP00000283871.5:p.Asp89Ala
ENST00000466528.5:n.292A>C
ENST00000476082.2:c.143A>C	ENSP00000419560.2:p.Asp48Ala
ENST00000485313.5:n.374A>C
ENST00000488183.5:n.524A>C
NM_000187.3:c.266A>C	NP_000178.2:p.Asp89Ala
XM_005247412.1:c.266A>C	XP_005247469.1:p.Asp89Ala
XM_005247413.1:c.266A>C	XP_005247470.1:p.Asp89Ala
XM_005247414.3:c.266A>C	XP_005247471.1:p.Asp89Ala
XM_011512746.1:c.266A>C	XP_011511048.1:p.Asp89Ala
XM_005247412.2:c.266A>C	XP_005247469.1:p.Asp89Ala
XM_005247413.2:c.266A>C	XP_005247470.1:p.Asp89Ala
XM_005247414.5:c.266A>C	XP_005247471.1:p.Asp89Ala
XM_011512746.2:c.266A>C	XP_011511048.1:p.Asp89Ala
XM_017006277.2:c.-158A>C	XP_016861766.1:n.-158A>C
NM_000187.4:c.266A>C MANE Select	NP_000178.2:p.Asp89Ala