Canonical Allele Identifier: CA360813942

Gene: IRF1

Linked Data

• MyVariant Identifiers: chr5:g.131819719A>G (hg19) ; chr5:g.132484027A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132484027A>G , CM000667.2:g.132484027A>G	GRCh38
NC_000005.9:g.131819719A>G , CM000667.1:g.131819719A>G	GRCh37
NC_000005.8:g.131847618A>G	NCBI36
NG_011450.1:g.11747T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245414.9:c.902T>C MANE Select	ENSP00000245414.4:p.Met301Thr
ENST00000638452.2:c.-169+34338A>G	ENSP00000492349.2:n.-169+34338A>G
ENST00000638504.1:n.206+64087A>G
ENST00000638568.2:c.-311+34338A>G	ENSP00000491158.2:n.-311+34338A>G
ENST00000639899.1:n.289+34338A>G
ENST00000640655.2:c.-637-2165A>G	ENSP00000491596.2:n.-637-2165A>G
ENST00000679743.1:c.523T>C	ENSP00000505257.1:n.523T>C
ENST00000679786.1:n.130+2530T>C
ENST00000679860.1:c.190T>C
ENST00000679921.1:c.292+2530T>C	ENSP00000505766.1:n.292+2530T>C
ENST00000679945.1:n.130+2530T>C
ENST00000679964.1:n.50+1640T>C
ENST00000680139.1:c.716T>C	ENSP00000506148.1:p.Met239Thr
ENST00000680380.1:n.136+335T>C
ENST00000680562.1:c.350T>C	ENSP00000505853.1:p.Met117Thr
ENST00000680594.1:n.136+335T>C
ENST00000680903.1:c.779T>C	ENSP00000505720.1:p.Met260Thr
ENST00000681049.1:n.50+1640T>C
ENST00000681240.1:c.152T>C	ENSP00000506034.1:p.Met51Thr
ENST00000681336.1:c.149T>C	ENSP00000505242.1:p.Met50Thr
ENST00000681462.1:c.739T>C
ENST00000681595.1:c.463T>C	ENSP00000506023.1:n.463T>C
ENST00000681634.1:n.136+335T>C
ENST00000681694.1:c.214T>C	ENSP00000506552.1:n.214T>C
ENST00000681715.1:c.400T>C	ENSP00000506545.1:n.400T>C
ENST00000245414.8:c.902T>C	ENSP00000245414.4:p.Met301Thr
ENST00000405885.6:c.902T>C	ENSP00000384406.1:p.Met301Thr
ENST00000472045.1:n.4211T>C
NM_002198.2:c.902T>C	NP_002189.1:p.Met301Thr
XM_011543378.1:c.779T>C	XP_011541680.1:p.Met260Thr
XM_011543379.1:c.650T>C	XP_011541681.1:p.Met217Thr
XR_427711.2:n.963T>C
NM_001354924.1:c.779T>C	NP_001341853.1:p.Met260Thr
NM_001354925.1:c.716T>C	NP_001341854.1:p.Met239Thr
NR_149068.1:n.963T>C
XM_011543379.2:c.650T>C	XP_011541681.1:p.Met217Thr
NM_002198.3:c.902T>C MANE Select	NP_002189.1:p.Met301Thr