Canonical Allele Identifier: CA1718180497

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75986044C= , CM000669.2:g.75986044C=	GRCh38
NC_000007.13:g.75615362C= , CM000669.1:g.75615362C=	GRCh37
NC_000007.12:g.75453298C=	NCBI36
NG_008930.1:g.75943C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.1566C=	ENSP00000516446.1:p.Ala522=
ENST00000706544.1:c.1692C=	ENSP00000516442.1:p.Ala564=
ENST00000706545.1:c.1791C=	ENSP00000516443.1:p.Ala597=
ENST00000706546.1:c.1791C=	ENSP00000516444.1:p.Ala597=
ENST00000706547.1:c.1791C=	ENSP00000516445.1:p.Ala597=
ENST00000461988.6:c.1791C= MANE Select	ENSP00000419970.1:p.Ala597=
ENST00000394893.5:c.1791C=	ENSP00000378355.1:p.Ala597=
ENST00000412064.6:c.*109-16C=	ENSP00000404731.2:n.*109-16C=
ENST00000439269.1:c.1005C=	ENSP00000412490.1:p.Ala335=
ENST00000447222.5:c.1942C=
ENST00000454934.5:c.*1096C=	ENSP00000414263.1:n.*1096C=
ENST00000461988.5:c.1791C=	ENSP00000419970.1:p.Ala597=
ENST00000493973.1:n.402C=
NM_000941.2:c.1791C=	NP_000932.3:p.Ala597=
NM_000941.3:c.1791C=	NP_000932.3:p.Ala597=
NM_001367562.1:c.1791C=	NP_001354491.1:p.Ala597=
NM_001382655.1:c.1845C=	NP_001369584.1:p.Ala615=
NM_001382657.1:c.1791C=	NP_001369586.1:p.Ala597=
NM_001382658.1:c.1791C=	NP_001369587.1:p.Ala597=
NM_001382659.1:c.1791C=	NP_001369588.1:p.Ala597=
NM_001382662.1:c.1641C=	NP_001369591.1:p.Ala547=
NM_001367562.3:c.1782C=	NP_001354491.2:p.Ala594=
NM_001382655.3:c.1836C=	NP_001369584.2:p.Ala612=
NM_001382657.2:c.1782C=	NP_001369586.2:p.Ala594=
NM_001382658.3:c.1782C=	NP_001369587.2:p.Ala594=
NM_001382659.3:c.1782C=	NP_001369588.2:p.Ala594=
NM_001382662.3:c.1632C=	NP_001369591.2:p.Ala544=
NM_001395413.1:c.1782C= MANE Select	NP_001382342.1:p.Ala594=