Canonical Allele Identifier: CA2560140

Gene: HGD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120646269A>G , CM000665.2:g.120646269A>G	GRCh38
NC_000003.11:g.120365116A>G , CM000665.1:g.120365116A>G	GRCh37
NC_000003.10:g.121847806A>G	NCBI36
NG_011957.1:g.41213T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000187.4:c.647T>C MANE Select	NP_000178.2:p.Ile216Thr
ENST00000283871.10:c.647T>C MANE Select	ENSP00000283871.5:p.Ile216Thr
NM_000187.3:c.647T>C	NP_000178.2:p.Ile216Thr
ENST00000283871.9:c.647T>C	ENSP00000283871.5:p.Ile216Thr
ENST00000475447.2:c.178T>C
ENST00000492108.5:c.180+704T>C	ENSP00000419838.1:n.180+704T>C
ENST00000494453.1:c.67T>C
XM_005247412.1:c.549+704T>C	XP_005247469.1:n.549+704T>C
XM_005247412.2:c.549+704T>C	XP_005247469.1:n.549+704T>C
XM_005247413.1:c.647T>C	XP_005247470.1:p.Ile216Thr
XM_005247413.2:c.647T>C	XP_005247470.1:p.Ile216Thr
XM_005247414.3:c.647T>C	XP_005247471.1:p.Ile216Thr
XM_005247414.5:c.647T>C	XP_005247471.1:p.Ile216Thr
XM_011512746.1:c.647T>C	XP_011511048.1:p.Ile216Thr
XM_011512746.2:c.647T>C	XP_011511048.1:p.Ile216Thr
XM_017006277.2:c.224T>C	XP_016861766.1:p.Ile75Thr