Canonical Allele Identifier: CA354073707

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120357403G>C (hg19) ; chr3:g.120638556G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638556G>C , CM000665.2:g.120638556G>C	GRCh38
NC_000003.11:g.120357403G>C , CM000665.1:g.120357403G>C	GRCh37
NC_000003.10:g.121840093G>C	NCBI36
NG_011957.1:g.48926C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.905C>G MANE Select	ENSP00000283871.5:p.Thr302Ser
ENST00000283871.9:c.905C>G	ENSP00000283871.5:p.Thr302Ser
ENST00000470321.1:n.245C>G
ENST00000475447.2:c.307+3033C>G
ENST00000492108.5:c.285+3033C>G	ENSP00000419838.1:n.285+3033C>G
ENST00000494453.1:c.325C>G
NM_000187.3:c.905C>G	NP_000178.2:p.Thr302Ser
XM_005247412.1:c.680C>G	XP_005247469.1:p.Thr227Ser
XM_005247413.1:c.905C>G	XP_005247470.1:p.Thr302Ser
XM_011512746.1:c.879+3033C>G	XP_011511048.1:n.879+3033C>G
XM_005247412.2:c.680C>G	XP_005247469.1:p.Thr227Ser
XM_005247413.2:c.905C>G	XP_005247470.1:p.Thr302Ser
XM_011512746.2:c.879+3033C>G	XP_011511048.1:n.879+3033C>G
XM_017006277.2:c.482C>G	XP_016861766.1:p.Thr161Ser
NM_000187.4:c.905C>G MANE Select	NP_000178.2:p.Thr302Ser