Canonical Allele Identifier: CA354077997

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120369633G>A (hg19) ; chr3:g.120650786G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120650786G>A , CM000665.2:g.120650786G>A	GRCh38
NC_000003.11:g.120369633G>A , CM000665.1:g.120369633G>A	GRCh37
NC_000003.10:g.121852323G>A	NCBI36
NG_011957.1:g.36696C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.422C>T MANE Select	ENSP00000283871.5:p.Ser141Phe
ENST00000283871.9:c.422C>T	ENSP00000283871.5:p.Ser141Phe
ENST00000476082.2:c.299C>T	ENSP00000419560.2:p.Ser100Phe
ENST00000492108.5:c.53C>T	ENSP00000419838.1:p.Ser18Phe
NM_000187.3:c.422C>T	NP_000178.2:p.Ser141Phe
XM_005247412.1:c.422C>T	XP_005247469.1:p.Ser141Phe
XM_005247413.1:c.422C>T	XP_005247470.1:p.Ser141Phe
XM_005247414.3:c.422C>T	XP_005247471.1:p.Ser141Phe
XM_011512746.1:c.422C>T	XP_011511048.1:p.Ser141Phe
XM_005247412.2:c.422C>T	XP_005247469.1:p.Ser141Phe
XM_005247413.2:c.422C>T	XP_005247470.1:p.Ser141Phe
XM_005247414.5:c.422C>T	XP_005247471.1:p.Ser141Phe
XM_011512746.2:c.422C>T	XP_011511048.1:p.Ser141Phe
XM_017006277.2:c.-2C>T	XP_016861766.1:n.-2C>T
NM_000187.4:c.422C>T MANE Select	NP_000178.2:p.Ser141Phe