Canonical Allele Identifier: CA4304310

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75986168C>T , CM000669.2:g.75986168C>T	GRCh38
NC_000007.13:g.75615486C>T , CM000669.1:g.75615486C>T	GRCh37
NC_000007.12:g.75453422C>T	NCBI36
NG_008930.1:g.76067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.1600C>T	ENSP00000516446.1:p.Gln534Ter
ENST00000706544.1:c.1726C>T	ENSP00000516442.1:p.Gln576Ter
ENST00000706545.1:c.1825C>T	ENSP00000516443.1:p.Gln609Ter
ENST00000706546.1:c.1825C>T	ENSP00000516444.1:p.Gln609Ter
ENST00000706547.1:c.1825C>T	ENSP00000516445.1:p.Gln609Ter
ENST00000461988.6:c.1825C>T MANE Select	ENSP00000419970.1:p.Gln609Ter
ENST00000394893.5:c.1825C>T	ENSP00000378355.1:p.Gln609Ter
ENST00000412064.6:c.*127C>T	ENSP00000404731.2:n.*127C>T
ENST00000439269.1:c.1039C>T	ENSP00000412490.1:p.Gln347Ter
ENST00000447222.5:c.1976C>T
ENST00000454934.5:c.*1130C>T	ENSP00000414263.1:n.*1130C>T
ENST00000461988.5:c.1825C>T	ENSP00000419970.1:p.Gln609Ter
ENST00000493973.1:n.436C>T
NM_000941.2:c.1825C>T	NP_000932.3:p.Gln609Ter
NM_000941.3:c.1825C>T	NP_000932.3:p.Gln609Ter
NM_001367562.1:c.1825C>T	NP_001354491.1:p.Gln609Ter
NM_001382655.1:c.1879C>T	NP_001369584.1:p.Gln627Ter
NM_001382657.1:c.1825C>T	NP_001369586.1:p.Gln609Ter
NM_001382658.1:c.1825C>T	NP_001369587.1:p.Gln609Ter
NM_001382659.1:c.1825C>T	NP_001369588.1:p.Gln609Ter
NM_001382662.1:c.1675C>T	NP_001369591.1:p.Gln559Ter
NM_001367562.3:c.1816C>T	NP_001354491.2:p.Gln606Ter
NM_001382655.3:c.1870C>T	NP_001369584.2:p.Gln624Ter
NM_001382657.2:c.1816C>T	NP_001369586.2:p.Gln606Ter
NM_001382658.3:c.1816C>T	NP_001369587.2:p.Gln606Ter
NM_001382659.3:c.1816C>T	NP_001369588.2:p.Gln606Ter
NM_001382662.3:c.1666C>T	NP_001369591.2:p.Gln556Ter
NM_001395413.1:c.1816C>T MANE Select	NP_001382342.1:p.Gln606Ter