Canonical Allele Identifier: CA2580714582

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75985882C>G , CM000669.2:g.75985882C>G	GRCh38
NC_000007.13:g.75615200C>G , CM000669.1:g.75615200C>G	GRCh37
NC_000007.12:g.75453136C>G	NCBI36
NG_008930.1:g.75781C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.1444+33C>G	ENSP00000516446.1:n.1444+33C>G
ENST00000706544.1:c.1570+33C>G	ENSP00000516442.1:n.1570+33C>G
ENST00000706545.1:c.1669+33C>G	ENSP00000516443.1:n.1669+33C>G
ENST00000706546.1:c.1669+33C>G	ENSP00000516444.1:n.1669+33C>G
ENST00000706547.1:c.1669+33C>G	ENSP00000516445.1:n.1669+33C>G
ENST00000461988.6:c.1669+33C>G MANE Select	ENSP00000419970.1:n.1669+33C>G
ENST00000394893.5:c.1669+33C>G	ENSP00000378355.1:n.1669+33C>G
ENST00000412064.6:c.*109-178C>G	ENSP00000404731.2:n.*109-178C>G
ENST00000439269.1:c.883+33C>G	ENSP00000412490.1:n.883+33C>G
ENST00000447222.5:c.1820+33C>G
ENST00000454934.5:c.*974+33C>G	ENSP00000414263.1:n.*974+33C>G
ENST00000461988.5:c.1669+33C>G	ENSP00000419970.1:n.1669+33C>G
ENST00000493973.1:n.280+33C>G
NM_000941.2:c.1669+33C>G	NP_000932.3:n.1669+33C>G
NM_000941.3:c.1669+33C>G	NP_000932.3:n.1669+33C>G
NM_001367562.1:c.1669+33C>G	NP_001354491.1:n.1669+33C>G
NM_001382655.1:c.1723+33C>G	NP_001369584.1:n.1723+33C>G
NM_001382657.1:c.1669+33C>G	NP_001369586.1:n.1669+33C>G
NM_001382658.1:c.1669+33C>G	NP_001369587.1:n.1669+33C>G
NM_001382659.1:c.1669+33C>G	NP_001369588.1:n.1669+33C>G
NM_001382662.1:c.1519+33C>G	NP_001369591.1:n.1519+33C>G
NM_001367562.3:c.1660+33C>G	NP_001354491.2:n.1660+33C>G
NM_001382655.3:c.1714+33C>G	NP_001369584.2:n.1714+33C>G
NM_001382657.2:c.1660+33C>G	NP_001369586.2:n.1660+33C>G
NM_001382658.3:c.1660+33C>G	NP_001369587.2:n.1660+33C>G
NM_001382659.3:c.1660+33C>G	NP_001369588.2:n.1660+33C>G
NM_001382662.3:c.1510+33C>G	NP_001369591.2:n.1510+33C>G
NM_001395413.1:c.1660+33C>G MANE Select	NP_001382342.1:n.1660+33C>G