Canonical Allele Identifier: CA2776541606

Gene: POR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984974_75984975insTGAGCCT , CM000669.2:g.75984974_75984975insTGAGCCT	GRCh38
NC_000007.13:g.75614292_75614293insTGAGCCT , CM000669.1:g.75614292_75614293insTGAGCCT	GRCh37
NC_000007.12:g.75452228_75452229insTGAGCCT	NCBI36
NG_008930.1:g.74873_74874insTGAGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.1023+16_1023+17insTGAGCCT	ENSP00000516446.1:n.1023+16_1023+17insTGAGCCT
ENST00000706544.1:c.1149+16_1149+17insTGAGCCT	ENSP00000516442.1:n.1149+16_1149+17insTGAGCCT
ENST00000706545.1:c.1248+16_1248+17insTGAGCCT	ENSP00000516443.1:n.1248+16_1248+17insTGAGCCT
ENST00000706546.1:c.1248+16_1248+17insTGAGCCT	ENSP00000516444.1:n.1248+16_1248+17insTGAGCCT
ENST00000706547.1:c.1248+16_1248+17insTGAGCCT	ENSP00000516445.1:n.1248+16_1248+17insTGAGCCT
ENST00000461988.6:c.1248+16_1248+17insTGAGCCT MANE Select	ENSP00000419970.1:n.1248+16_1248+17insTGAGCCT
ENST00000394893.5:c.1248+16_1248+17insTGAGCCT	ENSP00000378355.1:n.1248+16_1248+17insTGAGCCT
ENST00000412064.6:c.*109-1086_*109-1085insTGAGCCT	ENSP00000404731.2:n.*109-1086_*109-1085insTGAGCCT
ENST00000439269.1:c.462+16_462+17insTGAGCCT	ENSP00000412490.1:n.462+16_462+17insTGAGCCT
ENST00000447222.5:c.1399+16_1399+17insTGAGCCT
ENST00000454934.5:c.*553+16_*553+17insTGAGCCT	ENSP00000414263.1:n.*553+16_*553+17insTGAGCCT
ENST00000461988.5:c.1248+16_1248+17insTGAGCCT	ENSP00000419970.1:n.1248+16_1248+17insTGAGCCT
ENST00000487247.5:n.603+16_603+17insTGAGCCT
ENST00000495770.1:n.250+16_250+17insTGAGCCT
ENST00000496888.5:n.622+16_622+17insTGAGCCT
NM_000941.2:c.1248+16_1248+17insTGAGCCT	NP_000932.3:n.1248+16_1248+17insTGAGCCT
NM_000941.3:c.1248+16_1248+17insTGAGCCT	NP_000932.3:n.1248+16_1248+17insTGAGCCT
NM_001367562.1:c.1248+16_1248+17insTGAGCCT	NP_001354491.1:n.1248+16_1248+17insTGAGCCT
NM_001382655.1:c.1302+16_1302+17insTGAGCCT	NP_001369584.1:n.1302+16_1302+17insTGAGCCT
NM_001382657.1:c.1248+16_1248+17insTGAGCCT	NP_001369586.1:n.1248+16_1248+17insTGAGCCT
NM_001382658.1:c.1248+16_1248+17insTGAGCCT	NP_001369587.1:n.1248+16_1248+17insTGAGCCT
NM_001382659.1:c.1248+16_1248+17insTGAGCCT	NP_001369588.1:n.1248+16_1248+17insTGAGCCT
NM_001382662.1:c.1248+16_1248+17insTGAGCCT	NP_001369591.1:n.1248+16_1248+17insTGAGCCT
NM_001367562.3:c.1239+16_1239+17insTGAGCCT	NP_001354491.2:n.1239+16_1239+17insTGAGCCT
NM_001382655.3:c.1293+16_1293+17insTGAGCCT	NP_001369584.2:n.1293+16_1293+17insTGAGCCT
NM_001382657.2:c.1239+16_1239+17insTGAGCCT	NP_001369586.2:n.1239+16_1239+17insTGAGCCT
NM_001382658.3:c.1239+16_1239+17insTGAGCCT	NP_001369587.2:n.1239+16_1239+17insTGAGCCT
NM_001382659.3:c.1239+16_1239+17insTGAGCCT	NP_001369588.2:n.1239+16_1239+17insTGAGCCT
NM_001382662.3:c.1239+16_1239+17insTGAGCCT	NP_001369591.2:n.1239+16_1239+17insTGAGCCT
NM_001395413.1:c.1239+16_1239+17insTGAGCCT MANE Select	NP_001382342.1:n.1239+16_1239+17insTGAGCCT