Canonical Allele Identifier: CA354073584

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120357371C>G (hg19) ; chr3:g.120638524C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638524C>G , CM000665.2:g.120638524C>G	GRCh38
NC_000003.11:g.120357371C>G , CM000665.1:g.120357371C>G	GRCh37
NC_000003.10:g.121840061C>G	NCBI36
NG_011957.1:g.48958G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.937G>C MANE Select	ENSP00000283871.5:p.Ala313Pro
ENST00000283871.9:c.937G>C	ENSP00000283871.5:p.Ala313Pro
ENST00000470321.1:n.277G>C
ENST00000475447.2:c.307+3065G>C
ENST00000492108.5:c.285+3065G>C	ENSP00000419838.1:n.285+3065G>C
ENST00000494453.1:c.357G>C
NM_000187.3:c.937G>C	NP_000178.2:p.Ala313Pro
XM_005247412.1:c.712G>C	XP_005247469.1:p.Ala238Pro
XM_005247413.1:c.937G>C	XP_005247470.1:p.Ala313Pro
XM_011512746.1:c.879+3065G>C	XP_011511048.1:n.879+3065G>C
XM_005247412.2:c.712G>C	XP_005247469.1:p.Ala238Pro
XM_005247413.2:c.937G>C	XP_005247470.1:p.Ala313Pro
XM_011512746.2:c.879+3065G>C	XP_011511048.1:n.879+3065G>C
XM_017006277.2:c.514G>C	XP_016861766.1:p.Ala172Pro
NM_000187.4:c.937G>C MANE Select	NP_000178.2:p.Ala313Pro