Canonical Allele Identifier: CA2617607534
Gene: OLR1 HGNC NCBI

Linked Data

gnomAD v4: 12-10159592-TTTCAA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159593_10159597del , CM000674.2:g.10159593_10159597del GRCh38
NC_000012.11:g.10312192_10312196del , CM000674.1:g.10312192_10312196del GRCh37
NC_000012.10:g.10203459_10203463del NCBI36
NG_016743.1:g.17595_17599del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309539.8:c.*283_*287del MANE Select ENSP00000309124.3:n.*283_*287del
ENST00000309539.7:c.*283_*287del ENSP00000309124.3:n.*283_*287del
ENST00000543993.5:c.*419_*423del ENSP00000445085.1:n.*419_*423del
ENST00000544577.5:c.*283_*287del ENSP00000444457.1:n.*283_*287del
NM_001172632.1:c.*419_*423del NP_001166103.1:n.*419_*423del
NM_001172633.1:c.*419_*423del NP_001166104.1:n.*419_*423del
NM_002543.3:c.*283_*287del NP_002534.1:n.*283_*287del
XM_011520682.1:c.*283_*287del XP_011518984.1:n.*283_*287del
XM_011520683.1:c.*435_*439del XP_011518985.1:n.*435_*439del
NM_002543.4:c.*283_*287del MANE Select NP_002534.1:n.*283_*287del
NM_001172632.2:c.*419_*423del NP_001166103.1:n.*419_*423del
NM_001172633.2:c.*419_*423del NP_001166104.1:n.*419_*423del
Search 100 bp 5'
Search 100 bp 3'