Canonical Allele Identifier: CA1897600583
Gene: GPR158 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.25501892G= , CM000672.2:g.25501892G= GRCh38
NC_000010.10:g.25790821G= , CM000672.1:g.25790821G= GRCh37
NC_000010.9:g.25830827G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376351.4:c.1404+35173G= MANE Select ENSP00000365529.3:n.1404+35173G=
ENST00000650135.1:c.1167+35173G= ENSP00000498176.1:n.1167+35173G=
ENST00000376351.3:c.1404+35173G= ENSP00000365529.3:n.1404+35173G=
NM_020752.2:c.1404+35173G= NP_065803.2:n.1404+35173G=
XR_930511.1:n.2088+35173G=
XR_930512.1:n.2088+35173G=
XM_017016452.2:c.-157+35173G= XP_016871941.1:n.-157+35173G=
XR_930512.3:n.2088+35173G=
NM_020752.3:c.1404+35173G= MANE Select NP_065803.2:n.1404+35173G=