Canonical Allele Identifier: CA1718177634

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75981072T= , CM000669.2:g.75981072T=	GRCh38
NC_000007.13:g.75610390T= , CM000669.1:g.75610390T=	GRCh37
NC_000007.12:g.75448326T=	NCBI36
NG_008930.1:g.70971T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001395413.1:c.532T= MANE Select	NP_001382342.1:p.Tyr178=
ENST00000461988.6:c.541T= MANE Select	ENSP00000419970.1:p.Tyr181=
NM_000941.2:c.541T=	NP_000932.3:p.Tyr181=
NM_000941.3:c.541T=	NP_000932.3:p.Tyr181=
NM_001367562.1:c.541T=	NP_001354491.1:p.Tyr181=
NM_001367562.3:c.532T=	NP_001354491.2:p.Tyr178=
NM_001382655.1:c.595T=	NP_001369584.1:p.Tyr199=
NM_001382655.3:c.586T=	NP_001369584.2:p.Tyr196=
NM_001382657.1:c.541T=	NP_001369586.1:p.Tyr181=
NM_001382657.2:c.532T=	NP_001369586.2:p.Tyr178=
NM_001382658.1:c.541T=	NP_001369587.1:p.Tyr181=
NM_001382658.3:c.532T=	NP_001369587.2:p.Tyr178=
NM_001382659.1:c.541T=	NP_001369588.1:p.Tyr181=
NM_001382659.3:c.532T=	NP_001369588.2:p.Tyr178=
NM_001382662.1:c.541T=	NP_001369591.1:p.Tyr181=
NM_001382662.3:c.532T=	NP_001369591.2:p.Tyr178=
ENST00000394893.5:c.541T=	ENSP00000378355.1:p.Tyr181=
ENST00000412064.6:c.541T=	ENSP00000404731.2:p.Tyr181=
ENST00000439963.5:c.541T=	ENSP00000390540.1:p.Tyr181=
ENST00000447222.5:c.692T=
ENST00000454934.5:c.517-445T=	ENSP00000414263.1:n.517-445T=
ENST00000460892.1:n.141T=
ENST00000461988.5:c.541T=	ENSP00000419970.1:p.Tyr181=
ENST00000475509.2:c.316T=	ENSP00000516446.1:p.Tyr106=
ENST00000706544.1:c.541T=	ENSP00000516442.1:p.Tyr181=
ENST00000706545.1:c.541T=	ENSP00000516443.1:p.Tyr181=
ENST00000706546.1:c.541T=	ENSP00000516444.1:p.Tyr181=
ENST00000706547.1:c.541T=	ENSP00000516445.1:p.Tyr181=