Canonical Allele Identifier: CA358812195

Gene: HPGD

Linked Data

• MyVariant Identifiers: chr4:g.175414432G>C (hg19) ; chr4:g.174493281G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174493281G>C , CM000666.2:g.174493281G>C	GRCh38
NC_000004.11:g.175414432G>C , CM000666.1:g.175414432G>C	GRCh37
NC_000004.10:g.175651007G>C	NCBI36
NG_011689.1:g.34361C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296522.11:c.532C>G MANE Select	ENSP00000296522.6:p.Leu178Val
ENST00000296521.11:c.499-1187C>G	ENSP00000296521.7:n.499-1187C>G
ENST00000296522.10:c.532C>G	ENSP00000296522.6:p.Leu178Val
ENST00000422112.6:c.328C>G	ENSP00000398720.2:p.Leu110Val
ENST00000506910.5:c.169C>G	ENSP00000423066.1:p.Leu57Val
ENST00000508330.5:c.*161C>G	ENSP00000425741.1:n.*161C>G
ENST00000509512.1:n.181C>G
ENST00000510835.5:c.*294C>G	ENSP00000427699.1:n.*294C>G
ENST00000510901.5:c.169C>G	ENSP00000422418.1:p.Leu57Val
ENST00000511499.5:n.316C>G
ENST00000514584.5:c.169C>G	ENSP00000423110.1:p.Leu57Val
ENST00000541923.5:c.169C>G	ENSP00000438017.1:p.Leu57Val
ENST00000542498.5:c.422-1187C>G	ENSP00000443644.1:n.422-1187C>G
NM_000860.5:c.532C>G	NP_000851.2:p.Leu178Val
NM_001145816.2:c.499-1187C>G	NP_001139288.1:n.499-1187C>G
NM_001256301.1:c.169C>G	NP_001243230.1:p.Leu57Val
NM_001256305.1:c.422-1187C>G	NP_001243234.1:n.422-1187C>G
NM_001256306.1:c.328C>G	NP_001243235.1:p.Leu110Val
NM_001256307.1:c.169C>G	NP_001243236.1:p.Leu57Val
NM_000860.6:c.532C>G MANE Select	NP_000851.2:p.Leu178Val
NM_001145816.3:c.499-1187C>G	NP_001139288.1:n.499-1187C>G
NM_001256305.2:c.422-1187C>G	NP_001243234.1:n.422-1187C>G
NM_001256306.2:c.328C>G	NP_001243235.1:p.Leu110Val
NM_001256307.2:c.169C>G	NP_001243236.1:p.Leu57Val