Canonical Allele Identifier: CA354077220

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120647049G>C , CM000665.2:g.120647049G>C	GRCh38
NC_000003.11:g.120365896G>C , CM000665.1:g.120365896G>C	GRCh37
NC_000003.10:g.121848586G>C	NCBI36
NG_011957.1:g.40433C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.473C>G MANE Select	NP_000178.2:p.Pro158Arg
ENST00000283871.10:c.473C>G MANE Select	ENSP00000283871.5:p.Pro158Arg
NM_000187.3:c.473C>G	NP_000178.2:p.Pro158Arg
ENST00000283871.9:c.473C>G	ENSP00000283871.5:p.Pro158Arg
ENST00000475447.2:c.4C>G
ENST00000476082.2:c.350C>G	ENSP00000419560.2:p.Pro117Arg
ENST00000492108.5:c.104C>G	ENSP00000419838.1:p.Pro35Arg
XM_005247412.1:c.473C>G	XP_005247469.1:p.Pro158Arg
XM_005247412.2:c.473C>G	XP_005247469.1:p.Pro158Arg
XM_005247413.1:c.473C>G	XP_005247470.1:p.Pro158Arg
XM_005247413.2:c.473C>G	XP_005247470.1:p.Pro158Arg
XM_005247414.3:c.473C>G	XP_005247471.1:p.Pro158Arg
XM_005247414.5:c.473C>G	XP_005247471.1:p.Pro158Arg
XM_011512746.1:c.473C>G	XP_011511048.1:p.Pro158Arg
XM_011512746.2:c.473C>G	XP_011511048.1:p.Pro158Arg
XM_017006277.2:c.50C>G	XP_016861766.1:p.Pro17Arg