Canonical Allele Identifier: CA2790133950

Gene: IRF7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613076_613095del , CM000673.2:g.613076_613095del	GRCh38
NC_000011.9:g.613076_613095del , CM000673.1:g.613076_613095del	GRCh37
NC_000011.8:g.603076_603095del	NCBI36
NG_029106.1:g.7907_7926del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348655.11:c.1175_1194del	ENSP00000331803.9:p.Gln392LeufsTer?
ENST00000469048.6:c.*541_*560del	ENSP00000434607.1:n.*541_*560del
ENST00000525445.6:c.1262_1281del MANE Select	ENSP00000434009.2:p.Gln421LeufsTer?
ENST00000528413.6:c.1212_1231del	ENSP00000497888.1:n.1212_1231del
ENST00000330243.9:c.1301_1320del	ENSP00000329411.5:p.Gln434LeufsTer?
ENST00000348655.10:c.1175_1194del	ENSP00000331803.9:p.Gln392LeufsTer?
ENST00000397566.5:c.1301_1320del	ENSP00000380697.1:p.Gln434LeufsTer?
ENST00000397570.5:c.1214_1233del	ENSP00000380700.2:p.Gln405LeufsTer?
ENST00000397574.6:c.1262_1281del	ENSP00000380704.2:p.Gln421LeufsTer?
ENST00000469048.5:c.*541_*560del	ENSP00000434607.1:n.*541_*560del
ENST00000525445.5:c.944_963del	ENSP00000434009.1:p.Gln315LeufsTer?
ENST00000528413.5:n.377_396del
ENST00000531912.1:n.499_518del
ENST00000532326.5:c.*388_*407del	ENSP00000436696.1:n.*388_*407del
ENST00000533182.5:c.*626_*645del	ENSP00000433903.1:n.*626_*645del
NM_001572.3:c.1262_1281del	NP_001563.2:p.Gln421LeufsTer?
NM_004029.2:c.1175_1194del	NP_004020.1:p.Gln392LeufsTer?
NM_004031.2:c.1301_1320del	NP_004022.2:p.Gln434LeufsTer?
XM_005252906.2:c.1301_1320del	XP_005252963.1:p.Gln434LeufsTer?
XM_005252907.2:c.1298_1317del	XP_005252964.1:p.Gln433LeufsTer?
XM_005252909.2:c.1214_1233del	XP_005252966.1:p.Gln405LeufsTer?
XM_011520066.1:c.1259_1278del	XP_011518368.1:p.Gln420LeufsTer?
NM_001572.4:c.1262_1281del	NP_001563.2:p.Gln421LeufsTer?
NM_004029.3:c.1175_1194del	NP_004020.1:p.Gln392LeufsTer?
NM_004031.3:c.1301_1320del	NP_004022.2:p.Gln434LeufsTer?
XM_005252907.3:c.1298_1317del	XP_005252964.1:p.Gln433LeufsTer?
XM_005252909.3:c.1214_1233del	XP_005252966.1:p.Gln405LeufsTer?
XM_011520066.3:c.1259_1278del	XP_011518368.1:p.Gln420LeufsTer?
XM_017017674.1:c.383_402del	XP_016873163.1:p.Gln128LeufsTer?
NM_001572.5:c.1262_1281del MANE Select	NP_001563.2:p.Gln421LeufsTer?
NM_004029.4:c.1175_1194del	NP_004020.1:p.Gln392LeufsTer?
NM_004031.4:c.1301_1320del	NP_004022.2:p.Gln434LeufsTer?