Canonical Allele Identifier: CA9580533

Gene: IRF3

Linked Data

• dbSNP Id: rs2304207
• ExAC: 19:50167726 C / G
• gnomAD v2: 19-50167726-C-G
• gnomAD v3: 19-49664469-C-G
• gnomAD v4: 19-49664469-C-G
• MyVariant Identifiers: chr19:g.50167726C>G (hg19) ; chr19:g.49664469C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49664469C>G , CM000681.2:g.49664469C>G	GRCh38
NC_000019.9:g.50167726C>G , CM000681.1:g.50167726C>G	GRCh37
NC_000019.8:g.54859538C>G	NCBI36
NG_031810.1:g.6407G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377139.8:c.165+205G>C MANE Select	ENSP00000366344.3:n.165+205G>C
ENST00000309877.11:c.165+205G>C	ENSP00000310127.6:n.165+205G>C
ENST00000377135.8:c.-273-955G>C	ENSP00000366339.5:n.-273-955G>C
ENST00000377139.7:c.165+205G>C	ENSP00000366344.3:n.165+205G>C
ENST00000442265.2:c.165+205G>C	ENSP00000400378.2:n.165+205G>C
ENST00000593337.5:c.165+205G>C	ENSP00000473176.1:n.165+205G>C
ENST00000593818.5:c.-274+84G>C	ENSP00000471517.1:n.-274+84G>C
ENST00000593922.5:c.-300G>C	ENSP00000472601.1:n.-300G>C
ENST00000594387.1:n.282+205G>C
ENST00000595034.5:c.-102+84G>C	ENSP00000469067.1:n.-102+84G>C
ENST00000595240.5:n.55G>C
ENST00000596756.5:c.165+205G>C	ENSP00000473128.1:n.165+205G>C
ENST00000596765.5:c.-102+1162G>C	ENSP00000470512.1:n.-102+1162G>C
ENST00000596788.1:c.171+84G>C
ENST00000596822.5:c.-273-955G>C	ENSP00000468911.1:n.-273-955G>C
ENST00000597180.1:n.207+118G>C
ENST00000597198.5:c.165+205G>C	ENSP00000469113.1:n.165+205G>C
ENST00000597636.5:c.165+205G>C	ENSP00000470436.1:n.165+205G>C
ENST00000598108.5:c.165+205G>C	ENSP00000472223.1:n.165+205G>C
ENST00000598808.5:c.-274+84G>C	ENSP00000472582.1:n.-274+84G>C
ENST00000599144.5:c.-102+1162G>C	ENSP00000470069.1:n.-102+1162G>C
ENST00000599223.5:c.165+205G>C	ENSP00000471358.1:n.165+205G>C
ENST00000600022.5:c.-273-955G>C	ENSP00000472700.1:n.-273-955G>C
ENST00000600453.1:c.165+205G>C	ENSP00000470905.1:n.165+205G>C
ENST00000600911.5:c.165+205G>C	ENSP00000470431.1:n.165+205G>C
ENST00000601291.5:c.165+205G>C	ENSP00000471896.1:n.165+205G>C
ENST00000601373.5:c.-273-955G>C	ENSP00000471402.1:n.-273-955G>C
ENST00000601809.5:c.165+205G>C	ENSP00000470140.1:n.165+205G>C
NM_001197122.1:c.165+205G>C	NP_001184051.1:n.165+205G>C
NM_001197123.1:c.34G>C	NP_001184052.1:p.Val12Leu
NM_001197124.1:c.165+205G>C	NP_001184053.1:n.165+205G>C
NM_001197125.1:c.-273-955G>C	NP_001184054.1:n.-273-955G>C
NM_001197126.1:c.-102+1162G>C	NP_001184055.1:n.-102+1162G>C
NM_001197127.1:c.-273-955G>C	NP_001184056.1:n.-273-955G>C
NM_001197128.1:c.-102+1162G>C	NP_001184057.1:n.-102+1162G>C
NM_001571.5:c.165+205G>C	NP_001562.1:n.165+205G>C
NR_045568.1:n.565+205G>C
XM_006723197.1:c.165+205G>C	XP_006723260.1:n.165+205G>C
XM_006723198.1:c.165+205G>C	XP_006723261.1:n.165+205G>C
XM_006723199.2:c.165+205G>C	XP_006723262.1:n.165+205G>C
XM_006723200.1:c.34G>C	XP_006723263.1:p.Val12Leu
XM_006723201.1:c.-273-955G>C	XP_006723264.1:n.-273-955G>C
XM_006723202.1:c.-274+118G>C	XP_006723265.1:n.-274+118G>C
XR_935819.1:n.1113+205G>C
XR_935820.1:n.1113+205G>C
XM_006723198.2:c.165+205G>C	XP_006723261.1:n.165+205G>C
XM_017026766.2:c.165+205G>C	XP_016882255.1:n.165+205G>C
XM_017026767.2:c.165+205G>C	XP_016882256.1:n.165+205G>C
XM_024451492.1:c.165+205G>C	XP_024307260.1:n.165+205G>C
XM_024451493.1:c.165+205G>C	XP_024307261.1:n.165+205G>C
XM_024451494.1:c.-274+84G>C	XP_024307262.1:n.-274+84G>C
XM_024451495.1:c.-274+84G>C	XP_024307263.1:n.-274+84G>C
XM_024451496.1:c.-274+84G>C	XP_024307264.1:n.-274+84G>C
XM_024451497.1:c.-274+84G>C	XP_024307265.1:n.-274+84G>C
XM_024451498.1:c.-274+84G>C	XP_024307266.1:n.-274+84G>C
XR_001753678.1:n.400+205G>C
XR_002958310.1:n.274+205G>C
XR_002958311.1:n.274+205G>C
XR_002958312.1:n.55G>C
NM_001571.6:c.165+205G>C MANE Select	NP_001562.1:n.165+205G>C
NM_001197122.2:c.165+205G>C	NP_001184051.1:n.165+205G>C
NM_001197123.2:c.34G>C	NP_001184052.1:p.Val12Leu
NM_001197124.2:c.165+205G>C	NP_001184053.1:n.165+205G>C
NM_001197126.2:c.-102+1162G>C	NP_001184055.1:n.-102+1162G>C
NM_001197127.2:c.-273-955G>C	NP_001184056.1:n.-273-955G>C
NM_001197128.2:c.-102+1162G>C	NP_001184057.1:n.-102+1162G>C
NR_045568.2:n.547+205G>C
NM_001197125.2:c.-273-955G>C	NP_001184054.1:n.-273-955G>C