Canonical Allele Identifier: CA2675210189

Gene: IRF1

Linked Data

• gnomAD v4: 5-132484157-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484157_132484158insT , CM000667.2:g.132484157_132484158insT	GRCh38
NC_000005.9:g.131819849_131819850insT , CM000667.1:g.131819849_131819850insT	GRCh37
NC_000005.8:g.131847748_131847749insT	NCBI36
NG_011450.1:g.11616_11617insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.854-83_854-82insA MANE Select	ENSP00000245414.4:n.854-83_854-82insA
ENST00000613424.5:c.*75-83_*75-82insA	ENSP00000480887.1:n.*75-83_*75-82insA
ENST00000638452.2:c.-169+34468_-169+34469insT	ENSP00000492349.2:n.-169+34468_-169+34469insT
ENST00000638504.1:n.206+64217_206+64218insT
ENST00000638568.2:c.-311+34468_-311+34469insT	ENSP00000491158.2:n.-311+34468_-311+34469insT
ENST00000639899.1:n.289+34468_289+34469insT
ENST00000640655.2:c.-637-2035_-637-2034insT	ENSP00000491596.2:n.-637-2035_-637-2034insT
ENST00000679743.1:c.475-83_475-82insA	ENSP00000505257.1:n.475-83_475-82insA
ENST00000679786.1:n.130+2399_130+2400insA
ENST00000679860.1:c.142-83_142-82insA
ENST00000679921.1:c.292+2399_292+2400insA	ENSP00000505766.1:n.292+2399_292+2400insA
ENST00000679945.1:n.130+2399_130+2400insA
ENST00000679964.1:n.50+1509_50+1510insA
ENST00000680139.1:c.668-83_668-82insA	ENSP00000506148.1:n.668-83_668-82insA
ENST00000680380.1:n.136+204_136+205insA
ENST00000680562.1:c.302-83_302-82insA	ENSP00000505853.1:n.302-83_302-82insA
ENST00000680594.1:n.136+204_136+205insA
ENST00000680903.1:c.731-83_731-82insA	ENSP00000505720.1:n.731-83_731-82insA
ENST00000681049.1:n.50+1509_50+1510insA
ENST00000681240.1:c.104-83_104-82insA	ENSP00000506034.1:n.104-83_104-82insA
ENST00000681336.1:c.137-119_137-118insA	ENSP00000505242.1:n.137-119_137-118insA
ENST00000681462.1:c.691-83_691-82insA
ENST00000681595.1:c.415-83_415-82insA	ENSP00000506023.1:n.415-83_415-82insA
ENST00000681634.1:n.136+204_136+205insA
ENST00000681694.1:c.166-83_166-82insA	ENSP00000506552.1:n.166-83_166-82insA
ENST00000681715.1:c.352-83_352-82insA	ENSP00000506545.1:n.352-83_352-82insA
ENST00000245414.8:c.854-83_854-82insA	ENSP00000245414.4:n.854-83_854-82insA
ENST00000405885.6:c.854-83_854-82insA	ENSP00000384406.1:n.854-83_854-82insA
ENST00000472045.1:n.4080_4081insA
ENST00000613424.4:c.*75-83_*75-82insA	ENSP00000480887.1:n.*75-83_*75-82insA
NM_002198.2:c.854-83_854-82insA	NP_002189.1:n.854-83_854-82insA
XM_011543378.1:c.731-83_731-82insA	XP_011541680.1:n.731-83_731-82insA
XM_011543379.1:c.602-83_602-82insA	XP_011541681.1:n.602-83_602-82insA
XR_427711.2:n.915-83_915-82insA
NM_001354924.1:c.731-83_731-82insA	NP_001341853.1:n.731-83_731-82insA
NM_001354925.1:c.668-83_668-82insA	NP_001341854.1:n.668-83_668-82insA
NR_149068.1:n.915-83_915-82insA
XM_011543379.2:c.602-83_602-82insA	XP_011541681.1:n.602-83_602-82insA
NM_002198.3:c.854-83_854-82insA MANE Select	NP_002189.1:n.854-83_854-82insA