Canonical Allele Identifier: CA1718177986

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75981683T= , CM000669.2:g.75981683T=	GRCh38
NC_000007.13:g.75611001T= , CM000669.1:g.75611001T=	GRCh37
NC_000007.12:g.75448937T=	NCBI36
NG_008930.1:g.71582T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.506+77T=	ENSP00000516446.1:n.506+77T=
ENST00000706544.1:c.731+77T=	ENSP00000516442.1:n.731+77T=
ENST00000706545.1:c.731+77T=	ENSP00000516443.1:n.731+77T=
ENST00000706546.1:c.731+77T=	ENSP00000516444.1:n.731+77T=
ENST00000706547.1:c.731+77T=	ENSP00000516445.1:n.731+77T=
ENST00000461988.6:c.731+77T= MANE Select	ENSP00000419970.1:n.731+77T=
ENST00000394893.5:c.731+77T=	ENSP00000378355.1:n.731+77T=
ENST00000412064.6:c.567-579T=	ENSP00000404731.2:n.567-579T=
ENST00000447222.5:c.882+77T=
ENST00000454934.5:c.*36+77T=	ENSP00000414263.1:n.*36+77T=
ENST00000460892.1:n.331+77T=
ENST00000461988.5:c.731+77T=	ENSP00000419970.1:n.731+77T=
NM_000941.2:c.731+77T=	NP_000932.3:n.731+77T=
NM_000941.3:c.731+77T=	NP_000932.3:n.731+77T=
NM_001367562.1:c.731+77T=	NP_001354491.1:n.731+77T=
NM_001382655.1:c.785+77T=	NP_001369584.1:n.785+77T=
NM_001382657.1:c.731+77T=	NP_001369586.1:n.731+77T=
NM_001382658.1:c.731+77T=	NP_001369587.1:n.731+77T=
NM_001382659.1:c.731+77T=	NP_001369588.1:n.731+77T=
NM_001382662.1:c.731+77T=	NP_001369591.1:n.731+77T=
NM_001367562.3:c.722+77T=	NP_001354491.2:n.722+77T=
NM_001382655.3:c.776+77T=	NP_001369584.2:n.776+77T=
NM_001382657.2:c.722+77T=	NP_001369586.2:n.722+77T=
NM_001382658.3:c.722+77T=	NP_001369587.2:n.722+77T=
NM_001382659.3:c.722+77T=	NP_001369588.2:n.722+77T=
NM_001382662.3:c.722+77T=	NP_001369591.2:n.722+77T=
NM_001395413.1:c.722+77T= MANE Select	NP_001382342.1:n.722+77T=