Canonical Allele Identifier: CA442443942

Gene: HPGD

Linked Data

• MyVariant Identifiers: chr4:g.175414435T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174493284T>G , CM000666.2:g.174493284T>G	GRCh38
NC_000004.11:g.175414435T>G , CM000666.1:g.175414435T>G	GRCh37
NC_000004.10:g.175651010T>G	NCBI36
NG_011689.1:g.34358A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296522.11:c.529A>C MANE Select	ENSP00000296522.6:p.Arg177=
ENST00000296521.11:c.499-1190A>C	ENSP00000296521.7:n.499-1190A>C
ENST00000296522.10:c.529A>C	ENSP00000296522.6:p.Arg177=
ENST00000422112.6:c.325A>C	ENSP00000398720.2:p.Arg109=
ENST00000506910.5:c.166A>C	ENSP00000423066.1:p.Arg56=
ENST00000508330.5:c.*158A>C	ENSP00000425741.1:n.*158A>C
ENST00000509512.1:n.178A>C
ENST00000510835.5:c.*291A>C	ENSP00000427699.1:n.*291A>C
ENST00000510901.5:c.166A>C	ENSP00000422418.1:p.Arg56=
ENST00000511499.5:n.313A>C
ENST00000514584.5:c.166A>C	ENSP00000423110.1:p.Arg56=
ENST00000541923.5:c.166A>C	ENSP00000438017.1:p.Arg56=
ENST00000542498.5:c.422-1190A>C	ENSP00000443644.1:n.422-1190A>C
NM_000860.5:c.529A>C	NP_000851.2:p.Arg177=
NM_001145816.2:c.499-1190A>C	NP_001139288.1:n.499-1190A>C
NM_001256301.1:c.166A>C	NP_001243230.1:p.Arg56=
NM_001256305.1:c.422-1190A>C	NP_001243234.1:n.422-1190A>C
NM_001256306.1:c.325A>C	NP_001243235.1:p.Arg109=
NM_001256307.1:c.166A>C	NP_001243236.1:p.Arg56=
NM_000860.6:c.529A>C MANE Select	NP_000851.2:p.Arg177=
NM_001145816.3:c.499-1190A>C	NP_001139288.1:n.499-1190A>C
NM_001256305.2:c.422-1190A>C	NP_001243234.1:n.422-1190A>C
NM_001256306.2:c.325A>C	NP_001243235.1:p.Arg109=
NM_001256307.2:c.166A>C	NP_001243236.1:p.Arg56=