Canonical Allele Identifier: CA1718180877
Gene: POR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75986648G= , CM000669.2:g.75986648G= GRCh38
NC_000007.13:g.75615966G= , CM000669.1:g.75615966G= GRCh37
NC_000007.12:g.75453902G= NCBI36
NG_008930.1:g.76547G=

Transcript Alleles

HGVS Amino-acid change
ENST00000475509.2:c.*167G= ENSP00000516446.1:n.*167G=
ENST00000706544.1:c.*167G= ENSP00000516442.1:n.*167G=
ENST00000706545.1:c.*167G= ENSP00000516443.1:n.*167G=
ENST00000706546.1:c.*167G= ENSP00000516444.1:n.*167G=
ENST00000706547.1:c.*167G= ENSP00000516445.1:n.*167G=
ENST00000461988.6:c.*167G= MANE Select ENSP00000419970.1:n.*167G=
ENST00000394893.5:c.*403G= ENSP00000378355.1:n.*403G=
ENST00000439269.1:c.*167G= ENSP00000412490.1:n.*167G=
ENST00000454934.5:c.*1515G= ENSP00000414263.1:n.*1515G=
ENST00000461988.5:c.*167G= ENSP00000419970.1:n.*167G=
ENST00000493973.1:n.821G=
NM_000941.2:c.*167G= NP_000932.3:n.*167G=
NM_000941.3:c.*167G= NP_000932.3:n.*167G=
NM_001367562.1:c.*167G= NP_001354491.1:n.*167G=
NM_001382655.1:c.*167G= NP_001369584.1:n.*167G=
NM_001382657.1:c.*167G= NP_001369586.1:n.*167G=
NM_001382658.1:c.*167G= NP_001369587.1:n.*167G=
NM_001382659.1:c.*167G= NP_001369588.1:n.*167G=
NM_001382662.1:c.*167G= NP_001369591.1:n.*167G=
NM_001367562.3:c.*167G= NP_001354491.2:n.*167G=
NM_001382655.3:c.*167G= NP_001369584.2:n.*167G=
NM_001382657.2:c.*167G= NP_001369586.2:n.*167G=
NM_001382658.3:c.*167G= NP_001369587.2:n.*167G=
NM_001382659.3:c.*167G= NP_001369588.2:n.*167G=
NM_001382662.3:c.*167G= NP_001369591.2:n.*167G=
NM_001395413.1:c.*167G= MANE Select NP_001382342.1:n.*167G=