Canonical Allele Identifier: CA2683381792

Gene: POR

Linked Data

• gnomAD v4: 7-75984743-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984744_75984745del , CM000669.2:g.75984744_75984745del	GRCh38
NC_000007.13:g.75614062_75614063del , CM000669.1:g.75614062_75614063del	GRCh37
NC_000007.12:g.75451998_75451999del	NCBI36
NG_008930.1:g.74643_74644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.842-33_842-32del	ENSP00000516446.1:n.842-33_842-32del
ENST00000706544.1:c.968-33_968-32del	ENSP00000516442.1:n.968-33_968-32del
ENST00000706545.1:c.1067-33_1067-32del	ENSP00000516443.1:n.1067-33_1067-32del
ENST00000706546.1:c.1067-33_1067-32del	ENSP00000516444.1:n.1067-33_1067-32del
ENST00000706547.1:c.1067-33_1067-32del	ENSP00000516445.1:n.1067-33_1067-32del
ENST00000461988.6:c.1067-33_1067-32del MANE Select	ENSP00000419970.1:n.1067-33_1067-32del
ENST00000394893.5:c.1067-33_1067-32del	ENSP00000378355.1:n.1067-33_1067-32del
ENST00000412064.6:c.*108+1108_*108+1109del	ENSP00000404731.2:n.*108+1108_*108+1109del
ENST00000439269.1:c.281-33_281-32del	ENSP00000412490.1:n.281-33_281-32del
ENST00000447222.5:c.1218-33_1218-32del
ENST00000454934.5:c.*372-33_*372-32del	ENSP00000414263.1:n.*372-33_*372-32del
ENST00000461988.5:c.1067-33_1067-32del	ENSP00000419970.1:n.1067-33_1067-32del
ENST00000487247.5:n.422-33_422-32del
ENST00000495770.1:n.69-33_69-32del
ENST00000496888.5:n.441-33_441-32del
NM_000941.2:c.1067-33_1067-32del	NP_000932.3:n.1067-33_1067-32del
NM_000941.3:c.1067-33_1067-32del	NP_000932.3:n.1067-33_1067-32del
NM_001367562.1:c.1067-33_1067-32del	NP_001354491.1:n.1067-33_1067-32del
NM_001382655.1:c.1121-33_1121-32del	NP_001369584.1:n.1121-33_1121-32del
NM_001382657.1:c.1067-33_1067-32del	NP_001369586.1:n.1067-33_1067-32del
NM_001382658.1:c.1067-33_1067-32del	NP_001369587.1:n.1067-33_1067-32del
NM_001382659.1:c.1067-33_1067-32del	NP_001369588.1:n.1067-33_1067-32del
NM_001382662.1:c.1067-33_1067-32del	NP_001369591.1:n.1067-33_1067-32del
NM_001367562.3:c.1058-33_1058-32del	NP_001354491.2:n.1058-33_1058-32del
NM_001382655.3:c.1112-33_1112-32del	NP_001369584.2:n.1112-33_1112-32del
NM_001382657.2:c.1058-33_1058-32del	NP_001369586.2:n.1058-33_1058-32del
NM_001382658.3:c.1058-33_1058-32del	NP_001369587.2:n.1058-33_1058-32del
NM_001382659.3:c.1058-33_1058-32del	NP_001369588.2:n.1058-33_1058-32del
NM_001382662.3:c.1058-33_1058-32del	NP_001369591.2:n.1058-33_1058-32del
NM_001395413.1:c.1058-33_1058-32del MANE Select	NP_001382342.1:n.1058-33_1058-32del