Canonical Allele Identifier: CA354076305

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646267C>A , CM000665.2:g.120646267C>A	GRCh38
NC_000003.11:g.120365114C>A , CM000665.1:g.120365114C>A	GRCh37
NC_000003.10:g.121847804C>A	NCBI36
NG_011957.1:g.41215G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.649G>T MANE Select	NP_000178.2:p.Gly217Trp
ENST00000283871.10:c.649G>T MANE Select	ENSP00000283871.5:p.Gly217Trp
NM_000187.3:c.649G>T	NP_000178.2:p.Gly217Trp
ENST00000283871.9:c.649G>T	ENSP00000283871.5:p.Gly217Trp
ENST00000475447.2:c.180G>T
ENST00000492108.5:c.180+706G>T	ENSP00000419838.1:n.180+706G>T
ENST00000494453.1:c.69G>T
XM_005247412.1:c.549+706G>T	XP_005247469.1:n.549+706G>T
XM_005247412.2:c.549+706G>T	XP_005247469.1:n.549+706G>T
XM_005247413.1:c.649G>T	XP_005247470.1:p.Gly217Trp
XM_005247413.2:c.649G>T	XP_005247470.1:p.Gly217Trp
XM_005247414.3:c.649G>T	XP_005247471.1:p.Asp217Tyr
XM_005247414.5:c.649G>T	XP_005247471.1:p.Asp217Tyr
XM_011512746.1:c.649G>T	XP_011511048.1:p.Gly217Trp
XM_011512746.2:c.649G>T	XP_011511048.1:p.Gly217Trp
XM_017006277.2:c.226G>T	XP_016861766.1:p.Gly76Trp