Canonical Allele Identifier: CA4304014
Gene: POR HGNC NCBI

Linked Data

dbSNP Id: rs782192787
gnomAD v2: 7-75614213-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75984895C>A , CM000669.2:g.75984895C>A GRCh38
NC_000007.13:g.75614213C>A , CM000669.1:g.75614213C>A GRCh37
NC_000007.12:g.75452149C>A NCBI36
NG_008930.1:g.74794C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000475509.2:c.960C>A ENSP00000516446.1:p.Tyr320Ter
ENST00000706544.1:c.1086C>A ENSP00000516442.1:p.Tyr362Ter
ENST00000706545.1:c.1185C>A ENSP00000516443.1:p.Tyr395Ter
ENST00000706546.1:c.1185C>A ENSP00000516444.1:p.Tyr395Ter
ENST00000706547.1:c.1185C>A ENSP00000516445.1:p.Tyr395Ter
ENST00000461988.6:c.1185C>A MANE Select ENSP00000419970.1:p.Tyr395Ter
ENST00000394893.5:c.1185C>A ENSP00000378355.1:p.Tyr395Ter
ENST00000412064.6:c.*109-1165C>A ENSP00000404731.2:n.*109-1165C>A
ENST00000439269.1:c.399C>A ENSP00000412490.1:p.Tyr133Ter
ENST00000447222.5:c.1336C>A
ENST00000454934.5:c.*490C>A ENSP00000414263.1:n.*490C>A
ENST00000461988.5:c.1185C>A ENSP00000419970.1:p.Tyr395Ter
ENST00000487247.5:n.540C>A
ENST00000495770.1:n.187C>A
ENST00000496888.5:n.559C>A
NM_000941.2:c.1185C>A NP_000932.3:p.Tyr395Ter
NM_000941.3:c.1185C>A NP_000932.3:p.Tyr395Ter
NM_001367562.1:c.1185C>A NP_001354491.1:p.Tyr395Ter
NM_001382655.1:c.1239C>A NP_001369584.1:p.Tyr413Ter
NM_001382657.1:c.1185C>A NP_001369586.1:p.Tyr395Ter
NM_001382658.1:c.1185C>A NP_001369587.1:p.Tyr395Ter
NM_001382659.1:c.1185C>A NP_001369588.1:p.Tyr395Ter
NM_001382662.1:c.1185C>A NP_001369591.1:p.Tyr395Ter
NM_001367562.3:c.1176C>A NP_001354491.2:p.Tyr392Ter
NM_001382655.3:c.1230C>A NP_001369584.2:p.Tyr410Ter
NM_001382657.2:c.1176C>A NP_001369586.2:p.Tyr392Ter
NM_001382658.3:c.1176C>A NP_001369587.2:p.Tyr392Ter
NM_001382659.3:c.1176C>A NP_001369588.2:p.Tyr392Ter
NM_001382662.3:c.1176C>A NP_001369591.2:p.Tyr392Ter
NM_001395413.1:c.1176C>A MANE Select NP_001382342.1:p.Tyr392Ter