Canonical Allele Identifier: CA2551388970

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984739_75984740insAGATGT , CM000669.2:g.75984739_75984740insAGATGT	GRCh38
NC_000007.13:g.75614057_75614058insAGATGT , CM000669.1:g.75614057_75614058insAGATGT	GRCh37
NC_000007.12:g.75451993_75451994insAGATGT	NCBI36
NG_008930.1:g.74638_74639insAGATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.842-38_842-37insAGATGT	ENSP00000516446.1:n.842-38_842-37insAGATGT
ENST00000706544.1:c.968-38_968-37insAGATGT	ENSP00000516442.1:n.968-38_968-37insAGATGT
ENST00000706545.1:c.1067-38_1067-37insAGATGT	ENSP00000516443.1:n.1067-38_1067-37insAGATGT
ENST00000706546.1:c.1067-38_1067-37insAGATGT	ENSP00000516444.1:n.1067-38_1067-37insAGATGT
ENST00000706547.1:c.1067-38_1067-37insAGATGT	ENSP00000516445.1:n.1067-38_1067-37insAGATGT
ENST00000461988.6:c.1067-38_1067-37insAGATGT MANE Select	ENSP00000419970.1:n.1067-38_1067-37insAGATGT
ENST00000394893.5:c.1067-38_1067-37insAGATGT	ENSP00000378355.1:n.1067-38_1067-37insAGATGT
ENST00000412064.6:c.*108+1103_*108+1104insAGATGT	ENSP00000404731.2:n.*108+1103_*108+1104insAGATGT
ENST00000439269.1:c.281-38_281-37insAGATGT	ENSP00000412490.1:n.281-38_281-37insAGATGT
ENST00000447222.5:c.1218-38_1218-37insAGATGT
ENST00000454934.5:c.*372-38_*372-37insAGATGT	ENSP00000414263.1:n.*372-38_*372-37insAGATGT
ENST00000461988.5:c.1067-38_1067-37insAGATGT	ENSP00000419970.1:n.1067-38_1067-37insAGATGT
ENST00000487247.5:n.422-38_422-37insAGATGT
ENST00000495770.1:n.69-38_69-37insAGATGT
ENST00000496888.5:n.441-38_441-37insAGATGT
NM_000941.2:c.1067-38_1067-37insAGATGT	NP_000932.3:n.1067-38_1067-37insAGATGT
NM_000941.3:c.1067-38_1067-37insAGATGT	NP_000932.3:n.1067-38_1067-37insAGATGT
NM_001367562.1:c.1067-38_1067-37insAGATGT	NP_001354491.1:n.1067-38_1067-37insAGATGT
NM_001382655.1:c.1121-38_1121-37insAGATGT	NP_001369584.1:n.1121-38_1121-37insAGATGT
NM_001382657.1:c.1067-38_1067-37insAGATGT	NP_001369586.1:n.1067-38_1067-37insAGATGT
NM_001382658.1:c.1067-38_1067-37insAGATGT	NP_001369587.1:n.1067-38_1067-37insAGATGT
NM_001382659.1:c.1067-38_1067-37insAGATGT	NP_001369588.1:n.1067-38_1067-37insAGATGT
NM_001382662.1:c.1067-38_1067-37insAGATGT	NP_001369591.1:n.1067-38_1067-37insAGATGT
NM_001367562.3:c.1058-38_1058-37insAGATGT	NP_001354491.2:n.1058-38_1058-37insAGATGT
NM_001382655.3:c.1112-38_1112-37insAGATGT	NP_001369584.2:n.1112-38_1112-37insAGATGT
NM_001382657.2:c.1058-38_1058-37insAGATGT	NP_001369586.2:n.1058-38_1058-37insAGATGT
NM_001382658.3:c.1058-38_1058-37insAGATGT	NP_001369587.2:n.1058-38_1058-37insAGATGT
NM_001382659.3:c.1058-38_1058-37insAGATGT	NP_001369588.2:n.1058-38_1058-37insAGATGT
NM_001382662.3:c.1058-38_1058-37insAGATGT	NP_001369591.2:n.1058-38_1058-37insAGATGT
NM_001395413.1:c.1058-38_1058-37insAGATGT MANE Select	NP_001382342.1:n.1058-38_1058-37insAGATGT