Canonical Allele Identifier: CA472434235

Gene: IRF7

Linked Data

• MyVariant Identifiers: chr11:g.613098T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613098T>C , CM000673.2:g.613098T>C	GRCh38
NC_000011.9:g.613098T>C , CM000673.1:g.613098T>C	GRCh37
NC_000011.8:g.603098T>C	NCBI36
NG_029106.1:g.7902A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348655.11:c.1170A>G	ENSP00000331803.9:p.Ala390=
ENST00000469048.6:c.*536A>G	ENSP00000434607.1:n.*536A>G
ENST00000525445.6:c.1257A>G MANE Select	ENSP00000434009.2:p.Ala419=
ENST00000528413.6:c.1207A>G	ENSP00000497888.1:n.1207A>G
ENST00000330243.9:c.1296A>G	ENSP00000329411.5:p.Ala432=
ENST00000348655.10:c.1170A>G	ENSP00000331803.9:p.Ala390=
ENST00000397566.5:c.1296A>G	ENSP00000380697.1:p.Ala432=
ENST00000397570.5:c.1209A>G	ENSP00000380700.2:p.Ala403=
ENST00000397574.6:c.1257A>G	ENSP00000380704.2:p.Ala419=
ENST00000469048.5:c.*536A>G	ENSP00000434607.1:n.*536A>G
ENST00000525445.5:c.939A>G	ENSP00000434009.1:p.Ala313=
ENST00000528413.5:n.372A>G
ENST00000531912.1:n.494A>G
ENST00000532326.5:c.*383A>G	ENSP00000436696.1:n.*383A>G
ENST00000533182.5:c.*621A>G	ENSP00000433903.1:n.*621A>G
NM_001572.3:c.1257A>G	NP_001563.2:p.Ala419=
NM_004029.2:c.1170A>G	NP_004020.1:p.Ala390=
NM_004031.2:c.1296A>G	NP_004022.2:p.Ala432=
XM_005252906.2:c.1296A>G	XP_005252963.1:p.Ala432=
XM_005252907.2:c.1293A>G	XP_005252964.1:p.Ala431=
XM_005252909.2:c.1209A>G	XP_005252966.1:p.Ala403=
XM_011520066.1:c.1254A>G	XP_011518368.1:p.Ala418=
NM_001572.4:c.1257A>G	NP_001563.2:p.Ala419=
NM_004029.3:c.1170A>G	NP_004020.1:p.Ala390=
NM_004031.3:c.1296A>G	NP_004022.2:p.Ala432=
XM_005252907.3:c.1293A>G	XP_005252964.1:p.Ala431=
XM_005252909.3:c.1209A>G	XP_005252966.1:p.Ala403=
XM_011520066.3:c.1254A>G	XP_011518368.1:p.Ala418=
XM_017017674.1:c.378A>G	XP_016873163.1:p.Ala126=
NM_001572.5:c.1257A>G MANE Select	NP_001563.2:p.Ala419=
NM_004029.4:c.1170A>G	NP_004020.1:p.Ala390=
NM_004031.4:c.1296A>G	NP_004022.2:p.Ala432=