Canonical Allele Identifier: CA663230633
Gene: GPR158 HGNC NCBI

Linked Data

dbSNP Id: rs1340300190
gnomAD v3: 10-25591491-CT-C
gnomAD v4: 10-25591491-CT-C
MyVariant Identifiers: chr10:g.25880421del (hg19) chr10:g.25591492del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.25591493del , CM000672.2:g.25591493del GRCh38
NC_000010.10:g.25880422del , CM000672.1:g.25880422del GRCh37
NC_000010.9:g.25920428del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376351.4:c.1892+2348del MANE Select ENSP00000365529.3:n.1892+2348del
ENST00000650135.1:c.1655+2348del ENSP00000498176.1:n.1655+2348del
ENST00000376351.3:c.1892+2348del ENSP00000365529.3:n.1892+2348del
NM_020752.2:c.1892+2348del NP_065803.2:n.1892+2348del
XR_930511.1:n.2576+2348del
XR_930512.1:n.2576+2348del
XM_017016452.2:c.332+2348del XP_016871941.1:n.332+2348del
XR_930512.3:n.2576+2348del
NM_020752.3:c.1892+2348del MANE Select NP_065803.2:n.1892+2348del
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