Canonical Allele Identifier: CA1514328799

Gene: HPGD

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.174493211C= , CM000666.2:g.174493211C=	GRCh38
NC_000004.11:g.175414362C= , CM000666.1:g.175414362C=	GRCh37
NC_000004.10:g.175650937C=	NCBI36
NG_011689.1:g.34431G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296522.11:c.602G= MANE Select	ENSP00000296522.6:p.Gly201=
ENST00000296521.11:c.499-1117G=	ENSP00000296521.7:n.499-1117G=
ENST00000296522.10:c.602G=	ENSP00000296522.6:p.Gly201=
ENST00000422112.6:c.398G=	ENSP00000398720.2:p.Gly133=
ENST00000506910.5:c.239G=	ENSP00000423066.1:p.Gly80=
ENST00000508330.5:c.*231G=	ENSP00000425741.1:n.*231G=
ENST00000509512.1:n.251G=
ENST00000510835.5:c.*364G=	ENSP00000427699.1:n.*364G=
ENST00000510901.5:c.239G=	ENSP00000422418.1:p.Gly80=
ENST00000511499.5:n.386G=
ENST00000514584.5:c.239G=	ENSP00000423110.1:p.Gly80=
ENST00000541923.5:c.239G=	ENSP00000438017.1:p.Gly80=
ENST00000542498.5:c.422-1117G=	ENSP00000443644.1:n.422-1117G=
NM_000860.5:c.602G=	NP_000851.2:p.Gly201=
NM_001145816.2:c.499-1117G=	NP_001139288.1:n.499-1117G=
NM_001256301.1:c.239G=	NP_001243230.1:p.Gly80=
NM_001256305.1:c.422-1117G=	NP_001243234.1:n.422-1117G=
NM_001256306.1:c.398G=	NP_001243235.1:p.Gly133=
NM_001256307.1:c.239G=	NP_001243236.1:p.Gly80=
NM_000860.6:c.602G= MANE Select	NP_000851.2:p.Gly201=
NM_001145816.3:c.499-1117G=	NP_001139288.1:n.499-1117G=
NM_001256305.2:c.422-1117G=	NP_001243234.1:n.422-1117G=
NM_001256306.2:c.398G=	NP_001243235.1:p.Gly133=
NM_001256307.2:c.239G=	NP_001243236.1:p.Gly80=