Canonical Allele Identifier: CA2776541553
Gene: POR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75984685_75984686del , CM000669.2:g.75984685_75984686del GRCh38
NC_000007.13:g.75614003_75614004del , CM000669.1:g.75614003_75614004del GRCh37
NC_000007.12:g.75451939_75451940del NCBI36
NG_008930.1:g.74584_74585del

Transcript Alleles

HGVS Amino-acid Change
ENST00000475509.2:c.842-92_842-91del ENSP00000516446.1:n.842-92_842-91del
ENST00000706544.1:c.968-92_968-91del ENSP00000516442.1:n.968-92_968-91del
ENST00000706545.1:c.1067-92_1067-91del ENSP00000516443.1:n.1067-92_1067-91del
ENST00000706546.1:c.1067-92_1067-91del ENSP00000516444.1:n.1067-92_1067-91del
ENST00000706547.1:c.1067-92_1067-91del ENSP00000516445.1:n.1067-92_1067-91del
ENST00000461988.6:c.1067-92_1067-91del MANE Select ENSP00000419970.1:n.1067-92_1067-91del
ENST00000394893.5:c.1067-92_1067-91del ENSP00000378355.1:n.1067-92_1067-91del
ENST00000412064.6:c.*108+1049_*108+1050del ENSP00000404731.2:n.*108+1049_*108+1050del
ENST00000439269.1:c.281-92_281-91del ENSP00000412490.1:n.281-92_281-91del
ENST00000447222.5:c.1218-92_1218-91del
ENST00000454934.5:c.*372-92_*372-91del ENSP00000414263.1:n.*372-92_*372-91del
ENST00000461988.5:c.1067-92_1067-91del ENSP00000419970.1:n.1067-92_1067-91del
ENST00000487247.5:n.422-92_422-91del
ENST00000495770.1:n.69-92_69-91del
ENST00000496888.5:n.441-92_441-91del
NM_000941.2:c.1067-92_1067-91del NP_000932.3:n.1067-92_1067-91del
NM_000941.3:c.1067-92_1067-91del NP_000932.3:n.1067-92_1067-91del
NM_001367562.1:c.1067-92_1067-91del NP_001354491.1:n.1067-92_1067-91del
NM_001382655.1:c.1121-92_1121-91del NP_001369584.1:n.1121-92_1121-91del
NM_001382657.1:c.1067-92_1067-91del NP_001369586.1:n.1067-92_1067-91del
NM_001382658.1:c.1067-92_1067-91del NP_001369587.1:n.1067-92_1067-91del
NM_001382659.1:c.1067-92_1067-91del NP_001369588.1:n.1067-92_1067-91del
NM_001382662.1:c.1067-92_1067-91del NP_001369591.1:n.1067-92_1067-91del
NM_001367562.3:c.1058-92_1058-91del NP_001354491.2:n.1058-92_1058-91del
NM_001382655.3:c.1112-92_1112-91del NP_001369584.2:n.1112-92_1112-91del
NM_001382657.2:c.1058-92_1058-91del NP_001369586.2:n.1058-92_1058-91del
NM_001382658.3:c.1058-92_1058-91del NP_001369587.2:n.1058-92_1058-91del
NM_001382659.3:c.1058-92_1058-91del NP_001369588.2:n.1058-92_1058-91del
NM_001382662.3:c.1058-92_1058-91del NP_001369591.2:n.1058-92_1058-91del
NM_001395413.1:c.1058-92_1058-91del MANE Select NP_001382342.1:n.1058-92_1058-91del