Canonical Allele Identifier: CA1583185194

Gene: IRF1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484229C>G , CM000667.2:g.132484229C>G	GRCh38
NC_000005.9:g.131819921C>G , CM000667.1:g.131819921C>G	GRCh37
NC_000005.8:g.131847820C>G	NCBI36
NG_011450.1:g.11545G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.853+133G>C MANE Select	ENSP00000245414.4:n.853+133G>C
ENST00000613424.5:c.*74+133G>C	ENSP00000480887.1:n.*74+133G>C
ENST00000638452.2:c.-169+34540C>G	ENSP00000492349.2:n.-169+34540C>G
ENST00000638504.1:n.206+64289C>G
ENST00000638568.2:c.-311+34540C>G	ENSP00000491158.2:n.-311+34540C>G
ENST00000639899.1:n.289+34540C>G
ENST00000640655.2:c.-637-1963C>G	ENSP00000491596.2:n.-637-1963C>G
ENST00000679743.1:c.474+133G>C	ENSP00000505257.1:n.474+133G>C
ENST00000679786.1:n.130+2328G>C
ENST00000679860.1:c.142-154G>C
ENST00000679921.1:c.292+2328G>C	ENSP00000505766.1:n.292+2328G>C
ENST00000679945.1:n.130+2328G>C
ENST00000679964.1:n.50+1438G>C
ENST00000680139.1:c.668-154G>C	ENSP00000506148.1:n.668-154G>C
ENST00000680380.1:n.136+133G>C
ENST00000680562.1:c.301+133G>C	ENSP00000505853.1:n.301+133G>C
ENST00000680594.1:n.136+133G>C
ENST00000680903.1:c.730+133G>C	ENSP00000505720.1:n.730+133G>C
ENST00000681049.1:n.50+1438G>C
ENST00000681240.1:c.104-154G>C	ENSP00000506034.1:n.104-154G>C
ENST00000681336.1:c.136+133G>C	ENSP00000505242.1:n.136+133G>C
ENST00000681462.1:c.690+133G>C
ENST00000681595.1:c.414+133G>C	ENSP00000506023.1:n.414+133G>C
ENST00000681634.1:n.136+133G>C
ENST00000681694.1:c.166-154G>C	ENSP00000506552.1:n.166-154G>C
ENST00000681715.1:c.351+133G>C	ENSP00000506545.1:n.351+133G>C
ENST00000245414.8:c.853+133G>C	ENSP00000245414.4:n.853+133G>C
ENST00000405885.6:c.853+133G>C	ENSP00000384406.1:n.853+133G>C
ENST00000472045.1:n.4009G>C
ENST00000613424.4:c.*74+133G>C	ENSP00000480887.1:n.*74+133G>C
NM_002198.2:c.853+133G>C	NP_002189.1:n.853+133G>C
XM_011543378.1:c.730+133G>C	XP_011541680.1:n.730+133G>C
XM_011543379.1:c.601+133G>C	XP_011541681.1:n.601+133G>C
XR_427711.2:n.914+133G>C
NM_001354924.1:c.730+133G>C	NP_001341853.1:n.730+133G>C
NM_001354925.1:c.668-154G>C	NP_001341854.1:n.668-154G>C
NR_149068.1:n.914+133G>C
XM_011543379.2:c.601+133G>C	XP_011541681.1:n.601+133G>C
NM_002198.3:c.853+133G>C MANE Select	NP_002189.1:n.853+133G>C