Canonical Allele Identifier: CA1718179780

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984888C= , CM000669.2:g.75984888C=	GRCh38
NC_000007.13:g.75614206C= , CM000669.1:g.75614206C=	GRCh37
NC_000007.12:g.75452142C=	NCBI36
NG_008930.1:g.74787C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.953C=	ENSP00000516446.1:p.Ala318=
ENST00000706544.1:c.1079C=	ENSP00000516442.1:p.Ala360=
ENST00000706545.1:c.1178C=	ENSP00000516443.1:p.Ala393=
ENST00000706546.1:c.1178C=	ENSP00000516444.1:p.Ala393=
ENST00000706547.1:c.1178C=	ENSP00000516445.1:p.Ala393=
ENST00000461988.6:c.1178C= MANE Select	ENSP00000419970.1:p.Ala393=
ENST00000394893.5:c.1178C=	ENSP00000378355.1:p.Ala393=
ENST00000412064.6:c.*109-1172C=	ENSP00000404731.2:n.*109-1172C=
ENST00000439269.1:c.392C=	ENSP00000412490.1:p.Ala131=
ENST00000447222.5:c.1329C=
ENST00000454934.5:c.*483C=	ENSP00000414263.1:n.*483C=
ENST00000461988.5:c.1178C=	ENSP00000419970.1:p.Ala393=
ENST00000487247.5:n.533C=
ENST00000495770.1:n.180C=
ENST00000496888.5:n.552C=
NM_000941.2:c.1178C=	NP_000932.3:p.Ala393=
NM_000941.3:c.1178C=	NP_000932.3:p.Ala393=
NM_001367562.1:c.1178C=	NP_001354491.1:p.Ala393=
NM_001382655.1:c.1232C=	NP_001369584.1:p.Ala411=
NM_001382657.1:c.1178C=	NP_001369586.1:p.Ala393=
NM_001382658.1:c.1178C=	NP_001369587.1:p.Ala393=
NM_001382659.1:c.1178C=	NP_001369588.1:p.Ala393=
NM_001382662.1:c.1178C=	NP_001369591.1:p.Ala393=
NM_001367562.3:c.1169C=	NP_001354491.2:p.Ala390=
NM_001382655.3:c.1223C=	NP_001369584.2:p.Ala408=
NM_001382657.2:c.1169C=	NP_001369586.2:p.Ala390=
NM_001382658.3:c.1169C=	NP_001369587.2:p.Ala390=
NM_001382659.3:c.1169C=	NP_001369588.2:p.Ala390=
NM_001382662.3:c.1169C=	NP_001369591.2:p.Ala390=
NM_001395413.1:c.1169C= MANE Select	NP_001382342.1:p.Ala390=