Canonical Allele Identifier: CA360814027

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131819759C>A (hg19) ; chr5:g.132484067C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484067C>A , CM000667.2:g.132484067C>A	GRCh38
NC_000005.9:g.131819759C>A , CM000667.1:g.131819759C>A	GRCh37
NC_000005.8:g.131847658C>A	NCBI36
NG_011450.1:g.11707G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.862G>T MANE Select	ENSP00000245414.4:p.Gly288Trp
ENST00000613424.5:c.*83G>T	ENSP00000480887.1:n.*83G>T
ENST00000638452.2:c.-169+34378C>A	ENSP00000492349.2:n.-169+34378C>A
ENST00000638504.1:n.206+64127C>A
ENST00000638568.2:c.-311+34378C>A	ENSP00000491158.2:n.-311+34378C>A
ENST00000639899.1:n.289+34378C>A
ENST00000640655.2:c.-637-2125C>A	ENSP00000491596.2:n.-637-2125C>A
ENST00000679743.1:c.483G>T	ENSP00000505257.1:n.483G>T
ENST00000679786.1:n.130+2490G>T
ENST00000679860.1:c.150G>T
ENST00000679921.1:c.292+2490G>T	ENSP00000505766.1:n.292+2490G>T
ENST00000679945.1:n.130+2490G>T
ENST00000679964.1:n.50+1600G>T
ENST00000680139.1:c.676G>T	ENSP00000506148.1:p.Gly226Trp
ENST00000680380.1:n.136+295G>T
ENST00000680562.1:c.310G>T	ENSP00000505853.1:p.Gly104Trp
ENST00000680594.1:n.136+295G>T
ENST00000680903.1:c.739G>T	ENSP00000505720.1:p.Gly247Trp
ENST00000681049.1:n.50+1600G>T
ENST00000681240.1:c.112G>T	ENSP00000506034.1:p.Gly38Trp
ENST00000681336.1:c.137-28G>T	ENSP00000505242.1:n.137-28G>T
ENST00000681462.1:c.699G>T
ENST00000681595.1:c.423G>T	ENSP00000506023.1:n.423G>T
ENST00000681634.1:n.136+295G>T
ENST00000681694.1:c.174G>T	ENSP00000506552.1:p.Leu58Phe
ENST00000681715.1:c.360G>T	ENSP00000506545.1:n.360G>T
ENST00000245414.8:c.862G>T	ENSP00000245414.4:p.Gly288Trp
ENST00000405885.6:c.862G>T	ENSP00000384406.1:p.Gly288Trp
ENST00000472045.1:n.4171G>T
ENST00000613424.4:c.*83G>T	ENSP00000480887.1:n.*83G>T
NM_002198.2:c.862G>T	NP_002189.1:p.Gly288Trp
XM_011543378.1:c.739G>T	XP_011541680.1:p.Gly247Trp
XM_011543379.1:c.610G>T	XP_011541681.1:p.Gly204Trp
XR_427711.2:n.923G>T
NM_001354924.1:c.739G>T	NP_001341853.1:p.Gly247Trp
NM_001354925.1:c.676G>T	NP_001341854.1:p.Gly226Trp
NR_149068.1:n.923G>T
XM_011543379.2:c.610G>T	XP_011541681.1:p.Gly204Trp
NM_002198.3:c.862G>T MANE Select	NP_002189.1:p.Gly288Trp