Canonical Allele Identifier: CA435229723

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120389292A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120670445A>C , CM000665.2:g.120670445A>C	GRCh38
NC_000003.11:g.120389292A>C , CM000665.1:g.120389292A>C	GRCh37
NC_000003.10:g.121871982A>C	NCBI36
NG_011957.1:g.17037T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.264T>G MANE Select	ENSP00000283871.5:p.Val88=
ENST00000283871.9:c.264T>G	ENSP00000283871.5:p.Val88=
ENST00000466528.5:n.290T>G
ENST00000476082.2:c.141T>G	ENSP00000419560.2:p.Val47=
ENST00000485313.5:n.372T>G
ENST00000488183.5:n.522T>G
NM_000187.3:c.264T>G	NP_000178.2:p.Val88=
XM_005247412.1:c.264T>G	XP_005247469.1:p.Val88=
XM_005247413.1:c.264T>G	XP_005247470.1:p.Val88=
XM_005247414.3:c.264T>G	XP_005247471.1:p.Val88=
XM_011512746.1:c.264T>G	XP_011511048.1:p.Val88=
XM_005247412.2:c.264T>G	XP_005247469.1:p.Val88=
XM_005247413.2:c.264T>G	XP_005247470.1:p.Val88=
XM_005247414.5:c.264T>G	XP_005247471.1:p.Val88=
XM_011512746.2:c.264T>G	XP_011511048.1:p.Val88=
XM_017006277.2:c.-160T>G	XP_016861766.1:n.-160T>G
NM_000187.4:c.264T>G MANE Select	NP_000178.2:p.Val88=