Canonical Allele Identifier: CA2672714488

Gene: HPGD

Linked Data

• gnomAD v4: 4-174493330-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174493330T>C , CM000666.2:g.174493330T>C	GRCh38
NC_000004.11:g.175414481T>C , CM000666.1:g.175414481T>C	GRCh37
NC_000004.10:g.175651056T>C	NCBI36
NG_011689.1:g.34312A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296522.11:c.499-16A>G MANE Select	ENSP00000296522.6:n.499-16A>G
ENST00000296521.11:c.499-1236A>G	ENSP00000296521.7:n.499-1236A>G
ENST00000296522.10:c.499-16A>G	ENSP00000296522.6:n.499-16A>G
ENST00000422112.6:c.295-16A>G	ENSP00000398720.2:n.295-16A>G
ENST00000506910.5:c.136-16A>G	ENSP00000423066.1:n.136-16A>G
ENST00000508330.5:c.*128-16A>G	ENSP00000425741.1:n.*128-16A>G
ENST00000509512.1:n.132A>G
ENST00000510835.5:c.*261-16A>G	ENSP00000427699.1:n.*261-16A>G
ENST00000510901.5:c.136-16A>G	ENSP00000422418.1:n.136-16A>G
ENST00000511499.5:n.283-16A>G
ENST00000514584.5:c.136-16A>G	ENSP00000423110.1:n.136-16A>G
ENST00000541923.5:c.136-16A>G	ENSP00000438017.1:n.136-16A>G
ENST00000542498.5:c.422-1236A>G	ENSP00000443644.1:n.422-1236A>G
NM_000860.5:c.499-16A>G	NP_000851.2:n.499-16A>G
NM_001145816.2:c.499-1236A>G	NP_001139288.1:n.499-1236A>G
NM_001256301.1:c.136-16A>G	NP_001243230.1:n.136-16A>G
NM_001256305.1:c.422-1236A>G	NP_001243234.1:n.422-1236A>G
NM_001256306.1:c.295-16A>G	NP_001243235.1:n.295-16A>G
NM_001256307.1:c.136-16A>G	NP_001243236.1:n.136-16A>G
NM_000860.6:c.499-16A>G MANE Select	NP_000851.2:n.499-16A>G
NM_001145816.3:c.499-1236A>G	NP_001139288.1:n.499-1236A>G
NM_001256305.2:c.422-1236A>G	NP_001243234.1:n.422-1236A>G
NM_001256306.2:c.295-16A>G	NP_001243235.1:n.295-16A>G
NM_001256307.2:c.136-16A>G	NP_001243236.1:n.136-16A>G