Canonical Allele Identifier: CA3142295
Gene: HPGD HGNC NCBI

Linked Data

dbSNP Id: rs777346797

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174508707G>A , CM000666.2:g.174508707G>A GRCh38
NC_000004.11:g.175429858G>A , CM000666.1:g.175429858G>A GRCh37
NC_000004.10:g.175666433G>A NCBI36
NG_011689.1:g.18935C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296522.11:c.410C>T MANE Select ENSP00000296522.6:p.Ser137Leu
ENST00000296521.11:c.410C>T ENSP00000296521.7:p.Ser137Leu
ENST00000296522.10:c.410C>T ENSP00000296522.6:p.Ser137Leu
ENST00000422112.6:c.218-13083C>T ENSP00000398720.2:n.218-13083C>T
ENST00000504433.1:c.410C>T ENSP00000420892.1:p.Ser137Leu
ENST00000506910.5:c.47C>T ENSP00000423066.1:p.Ser16Leu
ENST00000508330.5:c.*39C>T ENSP00000425741.1:n.*39C>T
ENST00000510835.5:c.*172C>T ENSP00000427699.1:n.*172C>T
ENST00000510901.5:c.47C>T ENSP00000422418.1:p.Ser16Leu
ENST00000512410.1:n.391C>T
ENST00000514584.5:c.47C>T ENSP00000423110.1:p.Ser16Leu
ENST00000541923.5:c.47C>T ENSP00000438017.1:p.Ser16Leu
ENST00000542498.5:c.410C>T ENSP00000443644.1:p.Ser137Leu
NM_000860.5:c.410C>T NP_000851.2:p.Ser137Leu
NM_001145816.2:c.410C>T NP_001139288.1:p.Ser137Leu
NM_001256301.1:c.47C>T NP_001243230.1:p.Ser16Leu
NM_001256305.1:c.410C>T NP_001243234.1:p.Ser137Leu
NM_001256306.1:c.218-13083C>T NP_001243235.1:n.218-13083C>T
NM_001256307.1:c.47C>T NP_001243236.1:p.Ser16Leu
XM_011531907.1:c.410C>T XP_011530209.1:p.Ser137Leu
XR_938728.1:n.852C>T
NM_001363574.1:c.410C>T NP_001350503.1:p.Ser137Leu
XR_938728.2:n.447C>T
NM_000860.6:c.410C>T MANE Select NP_000851.2:p.Ser137Leu
NM_001363574.2:c.410C>T NP_001350503.1:p.Ser137Leu
NM_001145816.3:c.410C>T NP_001139288.1:p.Ser137Leu
NM_001256305.2:c.410C>T NP_001243234.1:p.Ser137Leu
NM_001256306.2:c.218-13083C>T NP_001243235.1:n.218-13083C>T
NM_001256307.2:c.47C>T NP_001243236.1:p.Ser16Leu