Canonical Allele Identifier: CA354073531

Gene: HGD

Linked Data

• gnomAD v4: 3-120638512-T-C
• MyVariant Identifiers: chr3:g.120357359T>C (hg19) ; chr3:g.120638512T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120638512T>C , CM000665.2:g.120638512T>C	GRCh38
NC_000003.11:g.120357359T>C , CM000665.1:g.120357359T>C	GRCh37
NC_000003.10:g.121840049T>C	NCBI36
NG_011957.1:g.48970A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.949A>G MANE Select	ENSP00000283871.5:p.Ile317Val
ENST00000283871.9:c.949A>G	ENSP00000283871.5:p.Ile317Val
ENST00000470321.1:n.289A>G
ENST00000475447.2:c.307+3077A>G
ENST00000492108.5:c.285+3077A>G	ENSP00000419838.1:n.285+3077A>G
ENST00000494453.1:c.369A>G
NM_000187.3:c.949A>G	NP_000178.2:p.Ile317Val
XM_005247412.1:c.724A>G	XP_005247469.1:p.Ile242Val
XM_005247413.1:c.949A>G	XP_005247470.1:p.Ile317Val
XM_011512746.1:c.879+3077A>G	XP_011511048.1:n.879+3077A>G
XM_005247412.2:c.724A>G	XP_005247469.1:p.Ile242Val
XM_005247413.2:c.949A>G	XP_005247470.1:p.Ile317Val
XM_011512746.2:c.879+3077A>G	XP_011511048.1:n.879+3077A>G
XM_017006277.2:c.526A>G	XP_016861766.1:p.Ile176Val
NM_000187.4:c.949A>G MANE Select	NP_000178.2:p.Ile317Val