Canonical Allele Identifier: CA354084277

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120682111T>C , CM000665.2:g.120682111T>C	GRCh38
NC_000003.11:g.120400958T>C , CM000665.1:g.120400958T>C	GRCh37
NC_000003.10:g.121883648T>C	NCBI36
NG_011957.1:g.5371A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.1A>G MANE Select	NP_000178.2:p.Met1Val
ENST00000283871.10:c.1A>G MANE Select	ENSP00000283871.5:p.Met1Val
NM_000187.3:c.1A>G	NP_000178.2:p.Met1Val
ENST00000283871.9:c.1A>G	ENSP00000283871.5:p.Met1Val
ENST00000466528.5:n.27A>G
ENST00000476082.2:c.-34A>G	ENSP00000419560.2:n.-34A>G
ENST00000480862.1:n.159A>G
ENST00000485313.5:n.21A>G
ENST00000488183.5:n.133A>G
XM_005247412.1:c.1A>G	XP_005247469.1:p.Met1Val
XM_005247412.2:c.1A>G	XP_005247469.1:p.Met1Val
XM_005247413.1:c.1A>G	XP_005247470.1:p.Met1Val
XM_005247413.2:c.1A>G	XP_005247470.1:p.Met1Val
XM_005247414.3:c.1A>G	XP_005247471.1:p.Met1Val
XM_005247414.5:c.1A>G	XP_005247471.1:p.Met1Val
XM_011512746.1:c.1A>G	XP_011511048.1:p.Met1Val
XM_011512746.2:c.1A>G	XP_011511048.1:p.Met1Val
XM_017006277.2:c.-511A>G	XP_016861766.1:n.-511A>G