Canonical Allele Identifier: CA2578915477

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75981620del , CM000669.2:g.75981620del	GRCh38
NC_000007.13:g.75610938del , CM000669.1:g.75610938del	GRCh37
NC_000007.12:g.75448874del	NCBI36
NG_008930.1:g.71519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.506+14del	ENSP00000516446.1:n.506+14del
ENST00000706544.1:c.731+14del	ENSP00000516442.1:n.731+14del
ENST00000706545.1:c.731+14del	ENSP00000516443.1:n.731+14del
ENST00000706546.1:c.731+14del	ENSP00000516444.1:n.731+14del
ENST00000706547.1:c.731+14del	ENSP00000516445.1:n.731+14del
ENST00000461988.6:c.731+14del MANE Select	ENSP00000419970.1:n.731+14del
ENST00000394893.5:c.731+14del	ENSP00000378355.1:n.731+14del
ENST00000412064.6:c.566+523del	ENSP00000404731.2:n.566+523del
ENST00000447222.5:c.882+14del
ENST00000454934.5:c.*36+14del	ENSP00000414263.1:n.*36+14del
ENST00000460892.1:n.331+14del
ENST00000461988.5:c.731+14del	ENSP00000419970.1:n.731+14del
NM_000941.2:c.731+14del	NP_000932.3:n.731+14del
NM_000941.3:c.731+14del	NP_000932.3:n.731+14del
NM_001367562.1:c.731+14del	NP_001354491.1:n.731+14del
NM_001382655.1:c.785+14del	NP_001369584.1:n.785+14del
NM_001382657.1:c.731+14del	NP_001369586.1:n.731+14del
NM_001382658.1:c.731+14del	NP_001369587.1:n.731+14del
NM_001382659.1:c.731+14del	NP_001369588.1:n.731+14del
NM_001382662.1:c.731+14del	NP_001369591.1:n.731+14del
NM_001367562.3:c.722+14del	NP_001354491.2:n.722+14del
NM_001382655.3:c.776+14del	NP_001369584.2:n.776+14del
NM_001382657.2:c.722+14del	NP_001369586.2:n.722+14del
NM_001382658.3:c.722+14del	NP_001369587.2:n.722+14del
NM_001382659.3:c.722+14del	NP_001369588.2:n.722+14del
NM_001382662.3:c.722+14del	NP_001369591.2:n.722+14del
NM_001395413.1:c.722+14del MANE Select	NP_001382342.1:n.722+14del