Canonical Allele Identifier: CA456330911

Gene: POR

Linked Data

• MyVariant Identifiers: chr7:g.75614192G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984874G>C , CM000669.2:g.75984874G>C	GRCh38
NC_000007.13:g.75614192G>C , CM000669.1:g.75614192G>C	GRCh37
NC_000007.12:g.75452128G>C	NCBI36
NG_008930.1:g.74773G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.939G>C	ENSP00000516446.1:p.Val313=
ENST00000706544.1:c.1065G>C	ENSP00000516442.1:p.Val355=
ENST00000706545.1:c.1164G>C	ENSP00000516443.1:p.Val388=
ENST00000706546.1:c.1164G>C	ENSP00000516444.1:p.Val388=
ENST00000706547.1:c.1164G>C	ENSP00000516445.1:p.Val388=
ENST00000461988.6:c.1164G>C MANE Select	ENSP00000419970.1:p.Val388=
ENST00000394893.5:c.1164G>C	ENSP00000378355.1:p.Val388=
ENST00000412064.6:c.*109-1186G>C	ENSP00000404731.2:n.*109-1186G>C
ENST00000439269.1:c.378G>C	ENSP00000412490.1:p.Val126=
ENST00000447222.5:c.1315G>C
ENST00000454934.5:c.*469G>C	ENSP00000414263.1:n.*469G>C
ENST00000461988.5:c.1164G>C	ENSP00000419970.1:p.Val388=
ENST00000487247.5:n.519G>C
ENST00000495770.1:n.166G>C
ENST00000496888.5:n.538G>C
NM_000941.2:c.1164G>C	NP_000932.3:p.Val388=
NM_000941.3:c.1164G>C	NP_000932.3:p.Val388=
NM_001367562.1:c.1164G>C	NP_001354491.1:p.Val388=
NM_001382655.1:c.1218G>C	NP_001369584.1:p.Val406=
NM_001382657.1:c.1164G>C	NP_001369586.1:p.Val388=
NM_001382658.1:c.1164G>C	NP_001369587.1:p.Val388=
NM_001382659.1:c.1164G>C	NP_001369588.1:p.Val388=
NM_001382662.1:c.1164G>C	NP_001369591.1:p.Val388=
NM_001367562.3:c.1155G>C	NP_001354491.2:p.Val385=
NM_001382655.3:c.1209G>C	NP_001369584.2:p.Val403=
NM_001382657.2:c.1155G>C	NP_001369586.2:p.Val385=
NM_001382658.3:c.1155G>C	NP_001369587.2:p.Val385=
NM_001382659.3:c.1155G>C	NP_001369588.2:p.Val385=
NM_001382662.3:c.1155G>C	NP_001369591.2:p.Val385=
NM_001395413.1:c.1155G>C MANE Select	NP_001382342.1:p.Val385=