Canonical Allele Identifier: CA803995274

Gene: IRF1

Linked Data

• dbSNP Id: rs1422579271
• MyVariant Identifiers: chr5:g.131819793_131819794insAAGA (hg19) ; chr5:g.132484101_132484102insAAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484102_132484103insAGAA , CM000667.2:g.132484102_132484103insAGAA	GRCh38
NC_000005.9:g.131819794_131819795insAGAA , CM000667.1:g.131819794_131819795insAGAA	GRCh37
NC_000005.8:g.131847693_131847694insAGAA	NCBI36
NG_011450.1:g.11672_11673insTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.854-27_854-26insTCTT MANE Select	ENSP00000245414.4:n.854-27_854-26insTCTT
ENST00000613424.5:c.*75-27_*75-26insTCTT	ENSP00000480887.1:n.*75-27_*75-26insTCTT
ENST00000638452.2:c.-169+34413_-169+34414insAGAA	ENSP00000492349.2:n.-169+34413_-169+34414insAGAA
ENST00000638504.1:n.206+64162_206+64163insAGAA
ENST00000638568.2:c.-311+34413_-311+34414insAGAA	ENSP00000491158.2:n.-311+34413_-311+34414insAGAA
ENST00000639899.1:n.289+34413_289+34414insAGAA
ENST00000640655.2:c.-637-2090_-637-2089insAGAA	ENSP00000491596.2:n.-637-2090_-637-2089insAGAA
ENST00000679743.1:c.475-27_475-26insTCTT	ENSP00000505257.1:n.475-27_475-26insTCTT
ENST00000679786.1:n.130+2455_130+2456insTCTT
ENST00000679860.1:c.142-27_142-26insTCTT
ENST00000679921.1:c.292+2455_292+2456insTCTT	ENSP00000505766.1:n.292+2455_292+2456insTCTT
ENST00000679945.1:n.130+2455_130+2456insTCTT
ENST00000679964.1:n.50+1565_50+1566insTCTT
ENST00000680139.1:c.668-27_668-26insTCTT	ENSP00000506148.1:n.668-27_668-26insTCTT
ENST00000680380.1:n.136+260_136+261insTCTT
ENST00000680562.1:c.302-27_302-26insTCTT	ENSP00000505853.1:n.302-27_302-26insTCTT
ENST00000680594.1:n.136+260_136+261insTCTT
ENST00000680903.1:c.731-27_731-26insTCTT	ENSP00000505720.1:n.731-27_731-26insTCTT
ENST00000681049.1:n.50+1565_50+1566insTCTT
ENST00000681240.1:c.104-27_104-26insTCTT	ENSP00000506034.1:n.104-27_104-26insTCTT
ENST00000681336.1:c.137-63_137-62insTCTT	ENSP00000505242.1:n.137-63_137-62insTCTT
ENST00000681462.1:c.691-27_691-26insTCTT
ENST00000681595.1:c.415-27_415-26insTCTT	ENSP00000506023.1:n.415-27_415-26insTCTT
ENST00000681634.1:n.136+260_136+261insTCTT
ENST00000681694.1:c.166-27_166-26insTCTT	ENSP00000506552.1:n.166-27_166-26insTCTT
ENST00000681715.1:c.352-27_352-26insTCTT	ENSP00000506545.1:n.352-27_352-26insTCTT
ENST00000245414.8:c.854-27_854-26insTCTT	ENSP00000245414.4:n.854-27_854-26insTCTT
ENST00000405885.6:c.854-27_854-26insTCTT	ENSP00000384406.1:n.854-27_854-26insTCTT
ENST00000472045.1:n.4136_4137insTCTT
ENST00000613424.4:c.*75-27_*75-26insTCTT	ENSP00000480887.1:n.*75-27_*75-26insTCTT
NM_002198.2:c.854-27_854-26insTCTT	NP_002189.1:n.854-27_854-26insTCTT
XM_011543378.1:c.731-27_731-26insTCTT	XP_011541680.1:n.731-27_731-26insTCTT
XM_011543379.1:c.602-27_602-26insTCTT	XP_011541681.1:n.602-27_602-26insTCTT
XR_427711.2:n.915-27_915-26insTCTT
NM_001354924.1:c.731-27_731-26insTCTT	NP_001341853.1:n.731-27_731-26insTCTT
NM_001354925.1:c.668-27_668-26insTCTT	NP_001341854.1:n.668-27_668-26insTCTT
NR_149068.1:n.915-27_915-26insTCTT
XM_011543379.2:c.602-27_602-26insTCTT	XP_011541681.1:n.602-27_602-26insTCTT
NM_002198.3:c.854-27_854-26insTCTT MANE Select	NP_002189.1:n.854-27_854-26insTCTT