Canonical Allele Identifier: CA354082537

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120394640T>A (hg19) ; chr3:g.120675793T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120675793T>A , CM000665.2:g.120675793T>A	GRCh38
NC_000003.11:g.120394640T>A , CM000665.1:g.120394640T>A	GRCh37
NC_000003.10:g.121877330T>A	NCBI36
NG_011957.1:g.11689A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283871.10:c.86A>T MANE Select	ENSP00000283871.5:p.Gln29Leu
ENST00000283871.9:c.86A>T	ENSP00000283871.5:p.Gln29Leu
ENST00000466528.5:n.112A>T
ENST00000476082.2:c.52A>T	ENSP00000419560.2:p.Ser18Cys
ENST00000480862.1:n.244A>T
ENST00000485313.5:n.194A>T
ENST00000488183.5:n.344A>T
NM_000187.3:c.86A>T	NP_000178.2:p.Gln29Leu
XM_005247412.1:c.86A>T	XP_005247469.1:p.Gln29Leu
XM_005247413.1:c.86A>T	XP_005247470.1:p.Gln29Leu
XM_005247414.3:c.86A>T	XP_005247471.1:p.Gln29Leu
XM_011512746.1:c.86A>T	XP_011511048.1:p.Gln29Leu
XM_005247412.2:c.86A>T	XP_005247469.1:p.Gln29Leu
XM_005247413.2:c.86A>T	XP_005247470.1:p.Gln29Leu
XM_005247414.5:c.86A>T	XP_005247471.1:p.Gln29Leu
XM_011512746.2:c.86A>T	XP_011511048.1:p.Gln29Leu
XM_017006277.2:c.-338A>T	XP_016861766.1:n.-338A>T
NM_000187.4:c.86A>T MANE Select	NP_000178.2:p.Gln29Leu