Canonical Allele Identifier: CA10629444

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75982324dup , CM000669.2:g.75982324dup	GRCh38
NC_000007.13:g.75611642dup , CM000669.1:g.75611642dup	GRCh37
NC_000007.12:g.75449578dup	NCBI36
NG_008930.1:g.72223dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.605+2dup	ENSP00000516446.1:n.605+2dup
ENST00000706544.1:c.731+718dup	ENSP00000516442.1:n.731+718dup
ENST00000706545.1:c.830+2dup	ENSP00000516443.1:n.830+2dup
ENST00000706546.1:c.830+2dup	ENSP00000516444.1:n.830+2dup
ENST00000706547.1:c.830+2dup	ENSP00000516445.1:n.830+2dup
ENST00000461988.6:c.830+2dup MANE Select	ENSP00000419970.1:n.830+2dup
ENST00000394893.5:c.830+2dup	ENSP00000378355.1:n.830+2dup
ENST00000412064.6:c.627+2dup	ENSP00000404731.2:n.627+2dup
ENST00000439269.1:c.44+2dup	ENSP00000412490.1:n.44+2dup
ENST00000447222.5:c.981+2dup
ENST00000454934.5:c.*135+2dup	ENSP00000414263.1:n.*135+2dup
ENST00000460892.1:n.430+2dup
ENST00000461988.5:c.830+2dup	ENSP00000419970.1:n.830+2dup
NM_000941.2:c.830+2dup	NP_000932.3:n.830+2dup
NM_000941.3:c.830+2dup	NP_000932.3:n.830+2dup
NM_001367562.1:c.830+2dup	NP_001354491.1:n.830+2dup
NM_001382655.1:c.884+2dup	NP_001369584.1:n.884+2dup
NM_001382657.1:c.830+2dup	NP_001369586.1:n.830+2dup
NM_001382658.1:c.830+2dup	NP_001369587.1:n.830+2dup
NM_001382659.1:c.830+2dup	NP_001369588.1:n.830+2dup
NM_001382662.1:c.830+2dup	NP_001369591.1:n.830+2dup
NM_001367562.3:c.821+2dup	NP_001354491.2:n.821+2dup
NM_001382655.3:c.875+2dup	NP_001369584.2:n.875+2dup
NM_001382657.2:c.821+2dup	NP_001369586.2:n.821+2dup
NM_001382658.3:c.821+2dup	NP_001369587.2:n.821+2dup
NM_001382659.3:c.821+2dup	NP_001369588.2:n.821+2dup
NM_001382662.3:c.821+2dup	NP_001369591.2:n.821+2dup
NM_001395413.1:c.821+2dup MANE Select	NP_001382342.1:n.821+2dup