Canonical Allele Identifier: CA367750407

Gene: POR

Linked Data

• gnomAD v4: 7-75985845-G-T
• MyVariant Identifiers: chr7:g.75615163G>T (hg19) ; chr7:g.75985845G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75985845G>T , CM000669.2:g.75985845G>T	GRCh38
NC_000007.13:g.75615163G>T , CM000669.1:g.75615163G>T	GRCh37
NC_000007.12:g.75453099G>T	NCBI36
NG_008930.1:g.75744G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.1440G>T	ENSP00000516446.1:p.Gln480His
ENST00000706544.1:c.1566G>T	ENSP00000516442.1:p.Gln522His
ENST00000706545.1:c.1665G>T	ENSP00000516443.1:p.Gln555His
ENST00000706546.1:c.1665G>T	ENSP00000516444.1:p.Gln555His
ENST00000706547.1:c.1665G>T	ENSP00000516445.1:p.Gln555His
ENST00000461988.6:c.1665G>T MANE Select	ENSP00000419970.1:p.Gln555His
ENST00000394893.5:c.1665G>T	ENSP00000378355.1:p.Gln555His
ENST00000412064.6:c.*109-215G>T	ENSP00000404731.2:n.*109-215G>T
ENST00000439269.1:c.879G>T	ENSP00000412490.1:p.Gln293His
ENST00000447222.5:c.1816G>T
ENST00000454934.5:c.*970G>T	ENSP00000414263.1:n.*970G>T
ENST00000461988.5:c.1665G>T	ENSP00000419970.1:p.Gln555His
ENST00000493973.1:n.276G>T
NM_000941.2:c.1665G>T	NP_000932.3:p.Gln555His
NM_000941.3:c.1665G>T	NP_000932.3:p.Gln555His
NM_001367562.1:c.1665G>T	NP_001354491.1:p.Gln555His
NM_001382655.1:c.1719G>T	NP_001369584.1:p.Gln573His
NM_001382657.1:c.1665G>T	NP_001369586.1:p.Gln555His
NM_001382658.1:c.1665G>T	NP_001369587.1:p.Gln555His
NM_001382659.1:c.1665G>T	NP_001369588.1:p.Gln555His
NM_001382662.1:c.1515G>T	NP_001369591.1:p.Gln505His
NM_001367562.3:c.1656G>T	NP_001354491.2:p.Gln552His
NM_001382655.3:c.1710G>T	NP_001369584.2:p.Gln570His
NM_001382657.2:c.1656G>T	NP_001369586.2:p.Gln552His
NM_001382658.3:c.1656G>T	NP_001369587.2:p.Gln552His
NM_001382659.3:c.1656G>T	NP_001369588.2:p.Gln552His
NM_001382662.3:c.1506G>T	NP_001369591.2:p.Gln502His
NM_001395413.1:c.1656G>T MANE Select	NP_001382342.1:p.Gln552His