Canonical Allele Identifier: CA367737491

Gene: POR

Linked Data

• MyVariant Identifiers: chr7:g.75583329T>G (hg19) ; chr7:g.75954011T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75954011T>G , CM000669.2:g.75954011T>G	GRCh38
NC_000007.13:g.75583329T>G , CM000669.1:g.75583329T>G	GRCh37
NC_000007.12:g.75421265T>G	NCBI36
NG_008930.1:g.43910T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706544.1:c.19T>G	ENSP00000516442.1:p.Ser7Ala
ENST00000706545.1:c.19T>G	ENSP00000516443.1:p.Ser7Ala
ENST00000706546.1:c.19T>G	ENSP00000516444.1:p.Ser7Ala
ENST00000706547.1:c.19T>G	ENSP00000516445.1:p.Ser7Ala
ENST00000461988.6:c.19T>G MANE Select	ENSP00000419970.1:p.Ser7Ala
ENST00000394893.5:c.19T>G	ENSP00000378355.1:p.Ser7Ala
ENST00000412064.6:c.19T>G	ENSP00000404731.2:p.Ser7Ala
ENST00000412521.5:c.19T>G	ENSP00000409238.1:p.Ser7Ala
ENST00000414186.5:c.19T>G	ENSP00000399327.1:p.Ser7Ala
ENST00000418341.1:c.19T>G	ENSP00000389719.1:p.Ser7Ala
ENST00000421059.1:c.19T>G	ENSP00000409881.1:p.Ser7Ala
ENST00000432753.5:c.19T>G	ENSP00000389409.1:p.Ser7Ala
ENST00000439963.5:c.19T>G	ENSP00000390540.1:p.Ser7Ala
ENST00000448410.5:c.19T>G	ENSP00000399409.1:p.Ser7Ala
ENST00000449920.5:c.19T>G	ENSP00000399556.1:p.Ser7Ala
ENST00000453773.5:c.19T>G	ENSP00000395813.1:p.Ser7Ala
ENST00000454934.5:c.19T>G	ENSP00000414263.1:p.Ser7Ala
ENST00000461988.5:c.19T>G	ENSP00000419970.1:p.Ser7Ala
ENST00000471238.5:n.46T>G
NM_000941.2:c.19T>G	NP_000932.3:p.Ser7Ala
NM_000941.3:c.19T>G	NP_000932.3:p.Ser7Ala
NM_001367562.1:c.19T>G	NP_001354491.1:p.Ser7Ala
NM_001382655.1:c.19T>G	NP_001369584.1:p.Ser7Ala
NM_001382657.1:c.19T>G	NP_001369586.1:p.Ser7Ala
NM_001382658.1:c.19T>G	NP_001369587.1:p.Ser7Ala
NM_001382659.1:c.19T>G	NP_001369588.1:p.Ser7Ala
NM_001382662.1:c.19T>G	NP_001369591.1:p.Ser7Ala
NM_001367562.3:c.10T>G	NP_001354491.2:p.Ser4Ala
NM_001382655.3:c.10T>G	NP_001369584.2:p.Ser4Ala
NM_001382657.2:c.10T>G	NP_001369586.2:p.Ser4Ala
NM_001382658.3:c.10T>G	NP_001369587.2:p.Ser4Ala
NM_001382659.3:c.10T>G	NP_001369588.2:p.Ser4Ala
NM_001382662.3:c.10T>G	NP_001369591.2:p.Ser4Ala
NM_001395413.1:c.10T>G MANE Select	NP_001382342.1:p.Ser4Ala