Canonical Allele Identifier: CA367749414

Gene: POR

Linked Data

• MyVariant Identifiers: chr7:g.75614211T>A (hg19) ; chr7:g.75984893T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984893T>A , CM000669.2:g.75984893T>A	GRCh38
NC_000007.13:g.75614211T>A , CM000669.1:g.75614211T>A	GRCh37
NC_000007.12:g.75452147T>A	NCBI36
NG_008930.1:g.74792T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.958T>A	ENSP00000516446.1:p.Tyr320Asn
ENST00000706544.1:c.1084T>A	ENSP00000516442.1:p.Tyr362Asn
ENST00000706545.1:c.1183T>A	ENSP00000516443.1:p.Tyr395Asn
ENST00000706546.1:c.1183T>A	ENSP00000516444.1:p.Tyr395Asn
ENST00000706547.1:c.1183T>A	ENSP00000516445.1:p.Tyr395Asn
ENST00000461988.6:c.1183T>A MANE Select	ENSP00000419970.1:p.Tyr395Asn
ENST00000394893.5:c.1183T>A	ENSP00000378355.1:p.Tyr395Asn
ENST00000412064.6:c.*109-1167T>A	ENSP00000404731.2:n.*109-1167T>A
ENST00000439269.1:c.397T>A	ENSP00000412490.1:p.Tyr133Asn
ENST00000447222.5:c.1334T>A
ENST00000454934.5:c.*488T>A	ENSP00000414263.1:n.*488T>A
ENST00000461988.5:c.1183T>A	ENSP00000419970.1:p.Tyr395Asn
ENST00000487247.5:n.538T>A
ENST00000495770.1:n.185T>A
ENST00000496888.5:n.557T>A
NM_000941.2:c.1183T>A	NP_000932.3:p.Tyr395Asn
NM_000941.3:c.1183T>A	NP_000932.3:p.Tyr395Asn
NM_001367562.1:c.1183T>A	NP_001354491.1:p.Tyr395Asn
NM_001382655.1:c.1237T>A	NP_001369584.1:p.Tyr413Asn
NM_001382657.1:c.1183T>A	NP_001369586.1:p.Tyr395Asn
NM_001382658.1:c.1183T>A	NP_001369587.1:p.Tyr395Asn
NM_001382659.1:c.1183T>A	NP_001369588.1:p.Tyr395Asn
NM_001382662.1:c.1183T>A	NP_001369591.1:p.Tyr395Asn
NM_001367562.3:c.1174T>A	NP_001354491.2:p.Tyr392Asn
NM_001382655.3:c.1228T>A	NP_001369584.2:p.Tyr410Asn
NM_001382657.2:c.1174T>A	NP_001369586.2:p.Tyr392Asn
NM_001382658.3:c.1174T>A	NP_001369587.2:p.Tyr392Asn
NM_001382659.3:c.1174T>A	NP_001369588.2:p.Tyr392Asn
NM_001382662.3:c.1174T>A	NP_001369591.2:p.Tyr392Asn
NM_001395413.1:c.1174T>A MANE Select	NP_001382342.1:p.Tyr392Asn