Canonical Allele Identifier: CA354081059

Gene: HGD

Linked Data

• MyVariant Identifiers: chr3:g.120389285C>A (hg19) ; chr3:g.120670438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120670438C>A , CM000665.2:g.120670438C>A	GRCh38
NC_000003.11:g.120389285C>A , CM000665.1:g.120389285C>A	GRCh37
NC_000003.10:g.121871975C>A	NCBI36
NG_011957.1:g.17044G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000283871.10:c.271G>T MANE Select	ENSP00000283871.5:p.Asp91Tyr
ENST00000283871.9:c.271G>T	ENSP00000283871.5:p.Asp91Tyr
ENST00000466528.5:n.297G>T
ENST00000476082.2:c.148G>T	ENSP00000419560.2:p.Asp50Tyr
ENST00000485313.5:n.379G>T
ENST00000488183.5:n.529G>T
NM_000187.3:c.271G>T	NP_000178.2:p.Asp91Tyr
XM_005247412.1:c.271G>T	XP_005247469.1:p.Asp91Tyr
XM_005247413.1:c.271G>T	XP_005247470.1:p.Asp91Tyr
XM_005247414.3:c.271G>T	XP_005247471.1:p.Asp91Tyr
XM_011512746.1:c.271G>T	XP_011511048.1:p.Asp91Tyr
XM_005247412.2:c.271G>T	XP_005247469.1:p.Asp91Tyr
XM_005247413.2:c.271G>T	XP_005247470.1:p.Asp91Tyr
XM_005247414.5:c.271G>T	XP_005247471.1:p.Asp91Tyr
XM_011512746.2:c.271G>T	XP_011511048.1:p.Asp91Tyr
XM_017006277.2:c.-153G>T	XP_016861766.1:n.-153G>T
NM_000187.4:c.271G>T MANE Select	NP_000178.2:p.Asp91Tyr