Canonical Allele Identifier: CA2617607687
Gene: OLR1 HGNC NCBI

Linked Data

gnomAD v4: 12-10159701-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159706del , CM000674.2:g.10159706del GRCh38
NC_000012.11:g.10312305del , CM000674.1:g.10312305del GRCh37
NC_000012.10:g.10203572del NCBI36
NG_016743.1:g.17490del

Transcript Alleles

HGVS Amino-acid change
ENST00000309539.8:c.*178del MANE Select ENSP00000309124.3:n.*178del
ENST00000309539.7:c.*178del ENSP00000309124.3:n.*178del
ENST00000432556.6:c.*314del ENSP00000405116.2:n.*314del
ENST00000536989.1:n.535del
ENST00000543993.5:c.*314del ENSP00000445085.1:n.*314del
ENST00000544577.5:c.*178del ENSP00000444457.1:n.*178del
ENST00000545927.5:c.*314del ENSP00000439251.1:n.*314del
NM_001172632.1:c.*314del NP_001166103.1:n.*314del
NM_001172633.1:c.*314del NP_001166104.1:n.*314del
NM_002543.3:c.*178del NP_002534.1:n.*178del
XM_011520682.1:c.*178del XP_011518984.1:n.*178del
XM_011520683.1:c.*330del XP_011518985.1:n.*330del
NM_002543.4:c.*178del MANE Select NP_002534.1:n.*178del
NM_001172632.2:c.*314del NP_001166103.1:n.*314del
NM_001172633.2:c.*314del NP_001166104.1:n.*314del
Search 100 bp 5'
Search 100 bp 3'