Canonical Allele Identifier: CA1897632612
Gene: GPR158 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.25591585C= , CM000672.2:g.25591585C= GRCh38
NC_000010.10:g.25880514C= , CM000672.1:g.25880514C= GRCh37
NC_000010.9:g.25920520C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376351.4:c.1892+2440C= MANE Select ENSP00000365529.3:n.1892+2440C=
ENST00000650135.1:c.1655+2440C= ENSP00000498176.1:n.1655+2440C=
ENST00000376351.3:c.1892+2440C= ENSP00000365529.3:n.1892+2440C=
NM_020752.2:c.1892+2440C= NP_065803.2:n.1892+2440C=
XR_930511.1:n.2576+2440C=
XR_930512.1:n.2576+2440C=
XM_017016452.2:c.332+2440C= XP_016871941.1:n.332+2440C=
XR_930512.3:n.2576+2440C=
NM_020752.3:c.1892+2440C= MANE Select NP_065803.2:n.1892+2440C=
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