Canonical Allele Identifier: CA2683384654

Gene: POR

Linked Data

• gnomAD v4: 7-75985859-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75985859G>C , CM000669.2:g.75985859G>C	GRCh38
NC_000007.13:g.75615177G>C , CM000669.1:g.75615177G>C	GRCh37
NC_000007.12:g.75453113G>C	NCBI36
NG_008930.1:g.75758G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.1444+10G>C	ENSP00000516446.1:n.1444+10G>C
ENST00000706544.1:c.1570+10G>C	ENSP00000516442.1:n.1570+10G>C
ENST00000706545.1:c.1669+10G>C	ENSP00000516443.1:n.1669+10G>C
ENST00000706546.1:c.1669+10G>C	ENSP00000516444.1:n.1669+10G>C
ENST00000706547.1:c.1669+10G>C	ENSP00000516445.1:n.1669+10G>C
ENST00000461988.6:c.1669+10G>C MANE Select	ENSP00000419970.1:n.1669+10G>C
ENST00000394893.5:c.1669+10G>C	ENSP00000378355.1:n.1669+10G>C
ENST00000412064.6:c.*109-201G>C	ENSP00000404731.2:n.*109-201G>C
ENST00000439269.1:c.883+10G>C	ENSP00000412490.1:n.883+10G>C
ENST00000447222.5:c.1820+10G>C
ENST00000454934.5:c.*974+10G>C	ENSP00000414263.1:n.*974+10G>C
ENST00000461988.5:c.1669+10G>C	ENSP00000419970.1:n.1669+10G>C
ENST00000493973.1:n.280+10G>C
NM_000941.2:c.1669+10G>C	NP_000932.3:n.1669+10G>C
NM_000941.3:c.1669+10G>C	NP_000932.3:n.1669+10G>C
NM_001367562.1:c.1669+10G>C	NP_001354491.1:n.1669+10G>C
NM_001382655.1:c.1723+10G>C	NP_001369584.1:n.1723+10G>C
NM_001382657.1:c.1669+10G>C	NP_001369586.1:n.1669+10G>C
NM_001382658.1:c.1669+10G>C	NP_001369587.1:n.1669+10G>C
NM_001382659.1:c.1669+10G>C	NP_001369588.1:n.1669+10G>C
NM_001382662.1:c.1519+10G>C	NP_001369591.1:n.1519+10G>C
NM_001367562.3:c.1660+10G>C	NP_001354491.2:n.1660+10G>C
NM_001382655.3:c.1714+10G>C	NP_001369584.2:n.1714+10G>C
NM_001382657.2:c.1660+10G>C	NP_001369586.2:n.1660+10G>C
NM_001382658.3:c.1660+10G>C	NP_001369587.2:n.1660+10G>C
NM_001382659.3:c.1660+10G>C	NP_001369588.2:n.1660+10G>C
NM_001382662.3:c.1510+10G>C	NP_001369591.2:n.1510+10G>C
NM_001395413.1:c.1660+10G>C MANE Select	NP_001382342.1:n.1660+10G>C