Canonical Allele Identifier: CA367750392

Gene: POR

Linked Data

• dbSNP Id: rs868908678
• gnomAD v4: 7-75985836-G-T
• MyVariant Identifiers: chr7:g.75615154G>T (hg19) ; chr7:g.75985836G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75985836G>T , CM000669.2:g.75985836G>T	GRCh38
NC_000007.13:g.75615154G>T , CM000669.1:g.75615154G>T	GRCh37
NC_000007.12:g.75453090G>T	NCBI36
NG_008930.1:g.75735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.1431G>T	ENSP00000516446.1:p.Trp477Cys
ENST00000706544.1:c.1557G>T	ENSP00000516442.1:p.Trp519Cys
ENST00000706545.1:c.1656G>T	ENSP00000516443.1:p.Trp552Cys
ENST00000706546.1:c.1656G>T	ENSP00000516444.1:p.Trp552Cys
ENST00000706547.1:c.1656G>T	ENSP00000516445.1:p.Trp552Cys
ENST00000461988.6:c.1656G>T MANE Select	ENSP00000419970.1:p.Trp552Cys
ENST00000394893.5:c.1656G>T	ENSP00000378355.1:p.Trp552Cys
ENST00000412064.6:c.*109-224G>T	ENSP00000404731.2:n.*109-224G>T
ENST00000439269.1:c.870G>T	ENSP00000412490.1:p.Trp290Cys
ENST00000447222.5:c.1807G>T
ENST00000454934.5:c.*961G>T	ENSP00000414263.1:n.*961G>T
ENST00000461988.5:c.1656G>T	ENSP00000419970.1:p.Trp552Cys
ENST00000493973.1:n.267G>T
NM_000941.2:c.1656G>T	NP_000932.3:p.Trp552Cys
NM_000941.3:c.1656G>T	NP_000932.3:p.Trp552Cys
NM_001367562.1:c.1656G>T	NP_001354491.1:p.Trp552Cys
NM_001382655.1:c.1710G>T	NP_001369584.1:p.Trp570Cys
NM_001382657.1:c.1656G>T	NP_001369586.1:p.Trp552Cys
NM_001382658.1:c.1656G>T	NP_001369587.1:p.Trp552Cys
NM_001382659.1:c.1656G>T	NP_001369588.1:p.Trp552Cys
NM_001382662.1:c.1506G>T	NP_001369591.1:p.Trp502Cys
NM_001367562.3:c.1647G>T	NP_001354491.2:p.Trp549Cys
NM_001382655.3:c.1701G>T	NP_001369584.2:p.Trp567Cys
NM_001382657.2:c.1647G>T	NP_001369586.2:p.Trp549Cys
NM_001382658.3:c.1647G>T	NP_001369587.2:p.Trp549Cys
NM_001382659.3:c.1647G>T	NP_001369588.2:p.Trp549Cys
NM_001382662.3:c.1497G>T	NP_001369591.2:p.Trp499Cys
NM_001395413.1:c.1647G>T MANE Select	NP_001382342.1:p.Trp549Cys