Canonical Allele Identifier: CA354074763

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120644318C>A , CM000665.2:g.120644318C>A	GRCh38
NC_000003.11:g.120363165C>A , CM000665.1:g.120363165C>A	GRCh37
NC_000003.10:g.121845855C>A	NCBI36
NG_011957.1:g.43164G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.774+1G>T MANE Select	NP_000178.2:n.774+1G>T
ENST00000283871.10:c.774+1G>T MANE Select	ENSP00000283871.5:n.774+1G>T
NM_000187.3:c.774+1G>T	NP_000178.2:n.774+1G>T
ENST00000283871.9:c.774+1G>T	ENSP00000283871.5:n.774+1G>T
ENST00000475447.2:c.202+280G>T
ENST00000492108.5:c.181-2625G>T	ENSP00000419838.1:n.181-2625G>T
ENST00000494453.1:c.194+1G>T
XM_005247412.1:c.550-2625G>T	XP_005247469.1:n.550-2625G>T
XM_005247412.2:c.550-2625G>T	XP_005247469.1:n.550-2625G>T
XM_005247413.1:c.774+1G>T	XP_005247470.1:n.774+1G>T
XM_005247413.2:c.774+1G>T	XP_005247470.1:n.774+1G>T
XM_011512746.1:c.774+1G>T	XP_011511048.1:n.774+1G>T
XM_011512746.2:c.774+1G>T	XP_011511048.1:n.774+1G>T
XM_017006277.2:c.351+1G>T	XP_016861766.1:n.351+1G>T