Canonical Allele Identifier: CA1718179722

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984787C= , CM000669.2:g.75984787C=	GRCh38
NC_000007.13:g.75614105C= , CM000669.1:g.75614105C=	GRCh37
NC_000007.12:g.75452041C=	NCBI36
NG_008930.1:g.74686C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.852C=	ENSP00000516446.1:p.Asn284=
ENST00000706544.1:c.978C=	ENSP00000516442.1:p.Asn326=
ENST00000706545.1:c.1077C=	ENSP00000516443.1:p.Asn359=
ENST00000706546.1:c.1077C=	ENSP00000516444.1:p.Asn359=
ENST00000706547.1:c.1077C=	ENSP00000516445.1:p.Asn359=
ENST00000461988.6:c.1077C= MANE Select	ENSP00000419970.1:p.Asn359=
ENST00000394893.5:c.1077C=	ENSP00000378355.1:p.Asn359=
ENST00000412064.6:c.*108+1151C=	ENSP00000404731.2:n.*108+1151C=
ENST00000439269.1:c.291C=	ENSP00000412490.1:p.Asn97=
ENST00000447222.5:c.1228C=
ENST00000454934.5:c.*382C=	ENSP00000414263.1:n.*382C=
ENST00000461988.5:c.1077C=	ENSP00000419970.1:p.Asn359=
ENST00000487247.5:n.432C=
ENST00000495770.1:n.79C=
ENST00000496888.5:n.451C=
NM_000941.2:c.1077C=	NP_000932.3:p.Asn359=
NM_000941.3:c.1077C=	NP_000932.3:p.Asn359=
NM_001367562.1:c.1077C=	NP_001354491.1:p.Asn359=
NM_001382655.1:c.1131C=	NP_001369584.1:p.Asn377=
NM_001382657.1:c.1077C=	NP_001369586.1:p.Asn359=
NM_001382658.1:c.1077C=	NP_001369587.1:p.Asn359=
NM_001382659.1:c.1077C=	NP_001369588.1:p.Asn359=
NM_001382662.1:c.1077C=	NP_001369591.1:p.Asn359=
NM_001367562.3:c.1068C=	NP_001354491.2:p.Asn356=
NM_001382655.3:c.1122C=	NP_001369584.2:p.Asn374=
NM_001382657.2:c.1068C=	NP_001369586.2:p.Asn356=
NM_001382658.3:c.1068C=	NP_001369587.2:p.Asn356=
NM_001382659.3:c.1068C=	NP_001369588.2:p.Asn356=
NM_001382662.3:c.1068C=	NP_001369591.2:p.Asn356=
NM_001395413.1:c.1068C= MANE Select	NP_001382342.1:p.Asn356=