Canonical Allele Identifier: CA435227723

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120644411A>G , CM000665.2:g.120644411A>G	GRCh38
NC_000003.11:g.120363258A>G , CM000665.1:g.120363258A>G	GRCh37
NC_000003.10:g.121845948A>G	NCBI36
NG_011957.1:g.43071T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.682T>C MANE Select	NP_000178.2:p.Leu228=
ENST00000283871.10:c.682T>C MANE Select	ENSP00000283871.5:p.Leu228=
NM_000187.3:c.682T>C	NP_000178.2:p.Leu228=
ENST00000283871.9:c.682T>C	ENSP00000283871.5:p.Leu228=
ENST00000475447.2:c.202+187T>C
ENST00000492108.5:c.180+2562T>C	ENSP00000419838.1:n.180+2562T>C
ENST00000494453.1:c.102T>C
XM_005247412.1:c.549+2562T>C	XP_005247469.1:n.549+2562T>C
XM_005247412.2:c.549+2562T>C	XP_005247469.1:n.549+2562T>C
XM_005247413.1:c.682T>C	XP_005247470.1:p.Leu228=
XM_005247413.2:c.682T>C	XP_005247470.1:p.Leu228=
XM_005247414.5:c.*156T>C	XP_005247471.1:n.*156T>C
XM_011512746.1:c.682T>C	XP_011511048.1:p.Leu228=
XM_011512746.2:c.682T>C	XP_011511048.1:p.Leu228=
XM_017006277.2:c.259T>C	XP_016861766.1:p.Leu87=