Canonical Allele Identifier: CA1718179731

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984801T= , CM000669.2:g.75984801T=	GRCh38
NC_000007.13:g.75614119T= , CM000669.1:g.75614119T=	GRCh37
NC_000007.12:g.75452055T=	NCBI36
NG_008930.1:g.74700T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.866T=	ENSP00000516446.1:p.Phe289=
ENST00000706544.1:c.992T=	ENSP00000516442.1:p.Phe331=
ENST00000706545.1:c.1091T=	ENSP00000516443.1:p.Phe364=
ENST00000706546.1:c.1091T=	ENSP00000516444.1:p.Phe364=
ENST00000706547.1:c.1091T=	ENSP00000516445.1:p.Phe364=
ENST00000461988.6:c.1091T= MANE Select	ENSP00000419970.1:p.Phe364=
ENST00000394893.5:c.1091T=	ENSP00000378355.1:p.Phe364=
ENST00000412064.6:c.*108+1165T=	ENSP00000404731.2:n.*108+1165T=
ENST00000439269.1:c.305T=	ENSP00000412490.1:p.Phe102=
ENST00000447222.5:c.1242T=
ENST00000454934.5:c.*396T=	ENSP00000414263.1:n.*396T=
ENST00000461988.5:c.1091T=	ENSP00000419970.1:p.Phe364=
ENST00000487247.5:n.446T=
ENST00000495770.1:n.93T=
ENST00000496888.5:n.465T=
NM_000941.2:c.1091T=	NP_000932.3:p.Phe364=
NM_000941.3:c.1091T=	NP_000932.3:p.Phe364=
NM_001367562.1:c.1091T=	NP_001354491.1:p.Phe364=
NM_001382655.1:c.1145T=	NP_001369584.1:p.Phe382=
NM_001382657.1:c.1091T=	NP_001369586.1:p.Phe364=
NM_001382658.1:c.1091T=	NP_001369587.1:p.Phe364=
NM_001382659.1:c.1091T=	NP_001369588.1:p.Phe364=
NM_001382662.1:c.1091T=	NP_001369591.1:p.Phe364=
NM_001367562.3:c.1082T=	NP_001354491.2:p.Phe361=
NM_001382655.3:c.1136T=	NP_001369584.2:p.Phe379=
NM_001382657.2:c.1082T=	NP_001369586.2:p.Phe361=
NM_001382658.3:c.1082T=	NP_001369587.2:p.Phe361=
NM_001382659.3:c.1082T=	NP_001369588.2:p.Phe361=
NM_001382662.3:c.1082T=	NP_001369591.2:p.Phe361=
NM_001395413.1:c.1082T= MANE Select	NP_001382342.1:p.Phe361=