Canonical Allele Identifier: CA4303988

Gene: POR

Linked Data

• ClinVar Variation Id: 360710
• ClinVar RCV Id: RCV000343979 ; RCV000878593
• dbSNP Id: rs150414675
• ExAC: 7:75614132 G / A
• gnomAD v2: 7-75614132-G-A
• gnomAD v3: 7-75984814-G-A
• gnomAD v4: 7-75984814-G-A
• MyVariant Identifiers: chr7:g.75614132G>A (hg19) ; chr7:g.75984814G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984814G>A , CM000669.2:g.75984814G>A	GRCh38
NC_000007.13:g.75614132G>A , CM000669.1:g.75614132G>A	GRCh37
NC_000007.12:g.75452068G>A	NCBI36
NG_008930.1:g.74713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.879G>A	ENSP00000516446.1:p.Thr293=
ENST00000706544.1:c.1005G>A	ENSP00000516442.1:p.Thr335=
ENST00000706545.1:c.1104G>A	ENSP00000516443.1:p.Thr368=
ENST00000706546.1:c.1104G>A	ENSP00000516444.1:p.Thr368=
ENST00000706547.1:c.1104G>A	ENSP00000516445.1:p.Thr368=
ENST00000461988.6:c.1104G>A MANE Select	ENSP00000419970.1:p.Thr368=
ENST00000394893.5:c.1104G>A	ENSP00000378355.1:p.Thr368=
ENST00000412064.6:c.*108+1178G>A	ENSP00000404731.2:n.*108+1178G>A
ENST00000439269.1:c.318G>A	ENSP00000412490.1:p.Thr106=
ENST00000447222.5:c.1255G>A
ENST00000454934.5:c.*409G>A	ENSP00000414263.1:n.*409G>A
ENST00000461988.5:c.1104G>A	ENSP00000419970.1:p.Thr368=
ENST00000487247.5:n.459G>A
ENST00000495770.1:n.106G>A
ENST00000496888.5:n.478G>A
NM_000941.2:c.1104G>A	NP_000932.3:p.Thr368=
NM_000941.3:c.1104G>A	NP_000932.3:p.Thr368=
NM_001367562.1:c.1104G>A	NP_001354491.1:p.Thr368=
NM_001382655.1:c.1158G>A	NP_001369584.1:p.Thr386=
NM_001382657.1:c.1104G>A	NP_001369586.1:p.Thr368=
NM_001382658.1:c.1104G>A	NP_001369587.1:p.Thr368=
NM_001382659.1:c.1104G>A	NP_001369588.1:p.Thr368=
NM_001382662.1:c.1104G>A	NP_001369591.1:p.Thr368=
NM_001367562.3:c.1095G>A	NP_001354491.2:p.Thr365=
NM_001382655.3:c.1149G>A	NP_001369584.2:p.Thr383=
NM_001382657.2:c.1095G>A	NP_001369586.2:p.Thr365=
NM_001382658.3:c.1095G>A	NP_001369587.2:p.Thr365=
NM_001382659.3:c.1095G>A	NP_001369588.2:p.Thr365=
NM_001382662.3:c.1095G>A	NP_001369591.2:p.Thr365=
NM_001395413.1:c.1095G>A MANE Select	NP_001382342.1:p.Thr365=