Canonical Allele Identifier: CA4303987
Gene: POR HGNC NCBI

Linked Data

dbSNP Id: rs377500167
gnomAD v2: 7-75614131-C-T
gnomAD v4: 7-75984813-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75984813C>T , CM000669.2:g.75984813C>T GRCh38
NC_000007.13:g.75614131C>T , CM000669.1:g.75614131C>T GRCh37
NC_000007.12:g.75452067C>T NCBI36
NG_008930.1:g.74712C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000475509.2:c.878C>T ENSP00000516446.1:p.Thr293Met
ENST00000706544.1:c.1004C>T ENSP00000516442.1:p.Thr335Met
ENST00000706545.1:c.1103C>T ENSP00000516443.1:p.Thr368Met
ENST00000706546.1:c.1103C>T ENSP00000516444.1:p.Thr368Met
ENST00000706547.1:c.1103C>T ENSP00000516445.1:p.Thr368Met
ENST00000461988.6:c.1103C>T MANE Select ENSP00000419970.1:p.Thr368Met
ENST00000394893.5:c.1103C>T ENSP00000378355.1:p.Thr368Met
ENST00000412064.6:c.*108+1177C>T ENSP00000404731.2:n.*108+1177C>T
ENST00000439269.1:c.317C>T ENSP00000412490.1:p.Thr106Met
ENST00000447222.5:c.1254C>T
ENST00000454934.5:c.*408C>T ENSP00000414263.1:n.*408C>T
ENST00000461988.5:c.1103C>T ENSP00000419970.1:p.Thr368Met
ENST00000487247.5:n.458C>T
ENST00000495770.1:n.105C>T
ENST00000496888.5:n.477C>T
NM_000941.2:c.1103C>T NP_000932.3:p.Thr368Met
NM_000941.3:c.1103C>T NP_000932.3:p.Thr368Met
NM_001367562.1:c.1103C>T NP_001354491.1:p.Thr368Met
NM_001382655.1:c.1157C>T NP_001369584.1:p.Thr386Met
NM_001382657.1:c.1103C>T NP_001369586.1:p.Thr368Met
NM_001382658.1:c.1103C>T NP_001369587.1:p.Thr368Met
NM_001382659.1:c.1103C>T NP_001369588.1:p.Thr368Met
NM_001382662.1:c.1103C>T NP_001369591.1:p.Thr368Met
NM_001367562.3:c.1094C>T NP_001354491.2:p.Thr365Met
NM_001382655.3:c.1148C>T NP_001369584.2:p.Thr383Met
NM_001382657.2:c.1094C>T NP_001369586.2:p.Thr365Met
NM_001382658.3:c.1094C>T NP_001369587.2:p.Thr365Met
NM_001382659.3:c.1094C>T NP_001369588.2:p.Thr365Met
NM_001382662.3:c.1094C>T NP_001369591.2:p.Thr365Met
NM_001395413.1:c.1094C>T MANE Select NP_001382342.1:p.Thr365Met