Canonical Allele Identifier: CA442443900

Gene: HPGD

Linked Data

• MyVariant Identifiers: chr4:g.175414382A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174493231A>G , CM000666.2:g.174493231A>G	GRCh38
NC_000004.11:g.175414382A>G , CM000666.1:g.175414382A>G	GRCh37
NC_000004.10:g.175650957A>G	NCBI36
NG_011689.1:g.34411T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296522.11:c.582T>C MANE Select	ENSP00000296522.6:p.Ile194=
ENST00000296521.11:c.499-1137T>C	ENSP00000296521.7:n.499-1137T>C
ENST00000296522.10:c.582T>C	ENSP00000296522.6:p.Ile194=
ENST00000422112.6:c.378T>C	ENSP00000398720.2:p.Ile126=
ENST00000506910.5:c.219T>C	ENSP00000423066.1:p.Ile73=
ENST00000508330.5:c.*211T>C	ENSP00000425741.1:n.*211T>C
ENST00000509512.1:n.231T>C
ENST00000510835.5:c.*344T>C	ENSP00000427699.1:n.*344T>C
ENST00000510901.5:c.219T>C	ENSP00000422418.1:p.Ile73=
ENST00000511499.5:n.366T>C
ENST00000514584.5:c.219T>C	ENSP00000423110.1:p.Ile73=
ENST00000541923.5:c.219T>C	ENSP00000438017.1:p.Ile73=
ENST00000542498.5:c.422-1137T>C	ENSP00000443644.1:n.422-1137T>C
NM_000860.5:c.582T>C	NP_000851.2:p.Ile194=
NM_001145816.2:c.499-1137T>C	NP_001139288.1:n.499-1137T>C
NM_001256301.1:c.219T>C	NP_001243230.1:p.Ile73=
NM_001256305.1:c.422-1137T>C	NP_001243234.1:n.422-1137T>C
NM_001256306.1:c.378T>C	NP_001243235.1:p.Ile126=
NM_001256307.1:c.219T>C	NP_001243236.1:p.Ile73=
NM_000860.6:c.582T>C MANE Select	NP_000851.2:p.Ile194=
NM_001145816.3:c.499-1137T>C	NP_001139288.1:n.499-1137T>C
NM_001256305.2:c.422-1137T>C	NP_001243234.1:n.422-1137T>C
NM_001256306.2:c.378T>C	NP_001243235.1:p.Ile126=
NM_001256307.2:c.219T>C	NP_001243236.1:p.Ile73=