Canonical Allele Identifier: CA354073851

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120360438C>G (hg19) ; chr3:g.120641591C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120641591C>G , CM000665.2:g.120641591C>G	GRCh38
NC_000003.11:g.120360438C>G , CM000665.1:g.120360438C>G	GRCh37
NC_000003.10:g.121843128C>G	NCBI36
NG_011957.1:g.45891G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.877G>C MANE Select	ENSP00000283871.5:p.Ala293Pro
ENST00000283871.9:c.877G>C	ENSP00000283871.5:p.Ala293Pro
ENST00000470321.1:n.217G>C
ENST00000475447.2:c.305G>C
ENST00000492108.5:c.283G>C	ENSP00000419838.1:p.Ala95Pro
ENST00000494453.1:c.297G>C
NM_000187.3:c.877G>C	NP_000178.2:p.Ala293Pro
XM_005247412.1:c.652G>C	XP_005247469.1:p.Ala218Pro
XM_005247413.1:c.877G>C	XP_005247470.1:p.Ala293Pro
XM_011512746.1:c.877G>C	XP_011511048.1:p.Ala293Pro
XM_005247412.2:c.652G>C	XP_005247469.1:p.Ala218Pro
XM_005247413.2:c.877G>C	XP_005247470.1:p.Ala293Pro
XM_011512746.2:c.877G>C	XP_011511048.1:p.Ala293Pro
XM_017006277.2:c.454G>C	XP_016861766.1:p.Ala152Pro
NM_000187.4:c.877G>C MANE Select	NP_000178.2:p.Ala293Pro