Canonical Allele Identifier: CA435228338

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120369635G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120650788G>C , CM000665.2:g.120650788G>C	GRCh38
NC_000003.11:g.120369635G>C , CM000665.1:g.120369635G>C	GRCh37
NC_000003.10:g.121852325G>C	NCBI36
NG_011957.1:g.36694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.420C>G MANE Select	ENSP00000283871.5:p.Thr140=
ENST00000283871.9:c.420C>G	ENSP00000283871.5:p.Thr140=
ENST00000476082.2:c.297C>G	ENSP00000419560.2:p.Thr99=
ENST00000485313.5:n.528C>G
ENST00000492108.5:c.51C>G	ENSP00000419838.1:p.Thr17=
NM_000187.3:c.420C>G	NP_000178.2:p.Thr140=
XM_005247412.1:c.420C>G	XP_005247469.1:p.Thr140=
XM_005247413.1:c.420C>G	XP_005247470.1:p.Thr140=
XM_005247414.3:c.420C>G	XP_005247471.1:p.Thr140=
XM_011512746.1:c.420C>G	XP_011511048.1:p.Thr140=
XM_005247412.2:c.420C>G	XP_005247469.1:p.Thr140=
XM_005247413.2:c.420C>G	XP_005247470.1:p.Thr140=
XM_005247414.5:c.420C>G	XP_005247471.1:p.Thr140=
XM_011512746.2:c.420C>G	XP_011511048.1:p.Thr140=
XM_017006277.2:c.-4C>G	XP_016861766.1:n.-4C>G
NM_000187.4:c.420C>G MANE Select	NP_000178.2:p.Thr140=