Canonical Allele Identifier: CA915948747

Gene: IRF7

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613207_613208delinsAC , CM000673.2:g.613207_613208delinsAC	GRCh38
NC_000011.9:g.613207_613208delinsAC , CM000673.1:g.613207_613208delinsAC	GRCh37
NC_000011.8:g.603207_603208delinsAC	NCBI36
NG_029106.1:g.7792_7793delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348655.11:c.1148_1149delinsGT	ENSP00000331803.9:p.Gln383Arg
ENST00000469048.6:c.*514_*515delinsGT	ENSP00000434607.1:n.*514_*515delinsGT
ENST00000525445.6:c.1235_1236delinsGT MANE Select	ENSP00000434009.2:p.Gln412Arg
ENST00000528413.6:c.1185_1186delinsGT	ENSP00000497888.1:n.1185_1186delinsGT
ENST00000330243.9:c.1274_1275delinsGT	ENSP00000329411.5:p.Gln425Arg
ENST00000348655.10:c.1148_1149delinsGT	ENSP00000331803.9:p.Gln383Arg
ENST00000397566.5:c.1274_1275delinsGT	ENSP00000380697.1:p.Gln425Arg
ENST00000397570.5:c.1187_1188delinsGT	ENSP00000380700.2:p.Gln396Arg
ENST00000397574.6:c.1235_1236delinsGT	ENSP00000380704.2:p.Gln412Arg
ENST00000469048.5:c.*514_*515delinsGT	ENSP00000434607.1:n.*514_*515delinsGT
ENST00000525445.5:c.917_918delinsGT	ENSP00000434009.1:p.Gln306Arg
ENST00000528413.5:n.338-76_338-75delinsGT
ENST00000531912.1:n.384_385delinsGT
ENST00000532326.5:c.*361_*362delinsGT	ENSP00000436696.1:n.*361_*362delinsGT
ENST00000533182.5:c.*599_*600delinsGT	ENSP00000433903.1:n.*599_*600delinsGT
NM_001572.3:c.1235_1236delinsGT	NP_001563.2:p.Gln412Arg
NM_004029.2:c.1148_1149delinsGT	NP_004020.1:p.Gln383Arg
NM_004031.2:c.1274_1275delinsGT	NP_004022.2:p.Gln425Arg
XM_005252906.2:c.1274_1275delinsGT	XP_005252963.1:p.Gln425Arg
XM_005252907.2:c.1271_1272delinsGT	XP_005252964.1:p.Gln424Arg
XM_005252909.2:c.1187_1188delinsGT	XP_005252966.1:p.Gln396Arg
XM_011520066.1:c.1232_1233delinsGT	XP_011518368.1:p.Gln411Arg
NM_001572.4:c.1235_1236delinsGT	NP_001563.2:p.Gln412Arg
NM_004029.3:c.1148_1149delinsGT	NP_004020.1:p.Gln383Arg
NM_004031.3:c.1274_1275delinsGT	NP_004022.2:p.Gln425Arg
XM_005252907.3:c.1271_1272delinsGT	XP_005252964.1:p.Gln424Arg
XM_005252909.3:c.1187_1188delinsGT	XP_005252966.1:p.Gln396Arg
XM_011520066.3:c.1232_1233delinsGT	XP_011518368.1:p.Gln411Arg
XM_017017674.1:c.356_357delinsGT	XP_016873163.1:p.Gln119Arg
NM_001572.5:c.1235_1236delinsGT MANE Select	NP_001563.2:p.Gln412Arg
NM_004029.4:c.1148_1149delinsGT	NP_004020.1:p.Gln383Arg
NM_004031.4:c.1274_1275delinsGT	NP_004022.2:p.Gln425Arg