Canonical Allele Identifier: CA2564521494

Gene: POR

Linked Data

• gnomAD v4: 7-75953930-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75953930C>G , CM000669.2:g.75953930C>G	GRCh38
NC_000007.13:g.75583248C>G , CM000669.1:g.75583248C>G	GRCh37
NC_000007.12:g.75421184C>G	NCBI36
NG_008930.1:g.43829C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706544.1:c.-4-59C>G	ENSP00000516442.1:n.-4-59C>G
ENST00000706545.1:c.-4-59C>G	ENSP00000516443.1:n.-4-59C>G
ENST00000706546.1:c.-4-59C>G	ENSP00000516444.1:n.-4-59C>G
ENST00000706547.1:c.-4-59C>G	ENSP00000516445.1:n.-4-59C>G
ENST00000461988.6:c.-4-59C>G MANE Select	ENSP00000419970.1:n.-4-59C>G
ENST00000394893.5:c.-4-59C>G	ENSP00000378355.1:n.-4-59C>G
ENST00000412521.5:c.-4-59C>G	ENSP00000409238.1:n.-4-59C>G
ENST00000414186.5:c.-4-59C>G	ENSP00000399327.1:n.-4-59C>G
ENST00000418341.1:c.-4-59C>G	ENSP00000389719.1:n.-4-59C>G
ENST00000421059.1:c.-4-59C>G	ENSP00000409881.1:n.-4-59C>G
ENST00000432753.5:c.-4-59C>G	ENSP00000389409.1:n.-4-59C>G
ENST00000439963.5:c.-4-59C>G	ENSP00000390540.1:n.-4-59C>G
ENST00000448410.5:c.-4-59C>G	ENSP00000399409.1:n.-4-59C>G
ENST00000449920.5:c.-4-59C>G	ENSP00000399556.1:n.-4-59C>G
ENST00000453773.5:c.-4-59C>G	ENSP00000395813.1:n.-4-59C>G
ENST00000461988.5:c.-4-59C>G	ENSP00000419970.1:n.-4-59C>G
ENST00000471238.5:n.24-59C>G
NM_000941.2:c.-4-59C>G	NP_000932.3:n.-4-59C>G
NM_000941.3:c.-4-59C>G	NP_000932.3:n.-4-59C>G
NM_001367562.1:c.-4-59C>G	NP_001354491.1:n.-4-59C>G
NM_001382655.1:c.-4-59C>G	NP_001369584.1:n.-4-59C>G
NM_001382657.1:c.-4-59C>G	NP_001369586.1:n.-4-59C>G
NM_001382658.1:c.-4-59C>G	NP_001369587.1:n.-4-59C>G
NM_001382659.1:c.-4-59C>G	NP_001369588.1:n.-4-59C>G
NM_001382662.1:c.-4-59C>G	NP_001369591.1:n.-4-59C>G
NM_001367562.3:c.-13-59C>G	NP_001354491.2:n.-13-59C>G
NM_001382655.3:c.-13-59C>G	NP_001369584.2:n.-13-59C>G
NM_001382657.2:c.-13-59C>G	NP_001369586.2:n.-13-59C>G
NM_001382658.3:c.-13-59C>G	NP_001369587.2:n.-13-59C>G
NM_001382659.3:c.-13-59C>G	NP_001369588.2:n.-13-59C>G
NM_001382662.3:c.-13-59C>G	NP_001369591.2:n.-13-59C>G
NM_001395413.1:c.-13-59C>G MANE Select	NP_001382342.1:n.-13-59C>G