Canonical Allele Identifier: CA1718179725
Gene: POR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75984789A= , CM000669.2:g.75984789A= GRCh38
NC_000007.13:g.75614107A= , CM000669.1:g.75614107A= GRCh37
NC_000007.12:g.75452043A= NCBI36
NG_008930.1:g.74688A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475509.2:c.854A= ENSP00000516446.1:p.Lys285=
ENST00000706544.1:c.980A= ENSP00000516442.1:p.Lys327=
ENST00000706545.1:c.1079A= ENSP00000516443.1:p.Lys360=
ENST00000706546.1:c.1079A= ENSP00000516444.1:p.Lys360=
ENST00000706547.1:c.1079A= ENSP00000516445.1:p.Lys360=
ENST00000461988.6:c.1079A= MANE Select ENSP00000419970.1:p.Lys360=
ENST00000394893.5:c.1079A= ENSP00000378355.1:p.Lys360=
ENST00000412064.6:c.*108+1153A= ENSP00000404731.2:n.*108+1153A=
ENST00000439269.1:c.293A= ENSP00000412490.1:p.Lys98=
ENST00000447222.5:c.1230A=
ENST00000454934.5:c.*384A= ENSP00000414263.1:n.*384A=
ENST00000461988.5:c.1079A= ENSP00000419970.1:p.Lys360=
ENST00000487247.5:n.434A=
ENST00000495770.1:n.81A=
ENST00000496888.5:n.453A=
NM_000941.2:c.1079A= NP_000932.3:p.Lys360=
NM_000941.3:c.1079A= NP_000932.3:p.Lys360=
NM_001367562.1:c.1079A= NP_001354491.1:p.Lys360=
NM_001382655.1:c.1133A= NP_001369584.1:p.Lys378=
NM_001382657.1:c.1079A= NP_001369586.1:p.Lys360=
NM_001382658.1:c.1079A= NP_001369587.1:p.Lys360=
NM_001382659.1:c.1079A= NP_001369588.1:p.Lys360=
NM_001382662.1:c.1079A= NP_001369591.1:p.Lys360=
NM_001367562.3:c.1070A= NP_001354491.2:p.Lys357=
NM_001382655.3:c.1124A= NP_001369584.2:p.Lys375=
NM_001382657.2:c.1070A= NP_001369586.2:p.Lys357=
NM_001382658.3:c.1070A= NP_001369587.2:p.Lys357=
NM_001382659.3:c.1070A= NP_001369588.2:p.Lys357=
NM_001382662.3:c.1070A= NP_001369591.2:p.Lys357=
NM_001395413.1:c.1070A= MANE Select NP_001382342.1:p.Lys357=