Canonical Allele Identifier: CA12482257
Gene: IRF5 HGNC NCBI

Linked Data

dbSNP Id: rs6953165

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128938156C>G , CM000669.2:g.128938156C>G GRCh38
NC_000007.13:g.128578210C>G , CM000669.1:g.128578210C>G GRCh37
NC_000007.12:g.128365446C>G NCBI36
NG_012306.1:g.5217C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000700148.1:n.52+322C>G
ENST00000357234.10:c.-12+107C>G MANE Select ENSP00000349770.5:n.-12+107C>G
ENST00000489702.6:c.-12+322C>G ENSP00000418037.2:n.-12+322C>G
ENST00000652142.1:n.21+107C>G
ENST00000652525.1:c.-12+462C>G ENSP00000498293.1:n.-12+462C>G
ENST00000357234.9:c.-12+107C>G ENSP00000349770.5:n.-12+107C>G
ENST00000402030.6:c.-12+107C>G ENSP00000385352.2:n.-12+107C>G
ENST00000461416.1:n.69+107C>G
ENST00000464557.5:c.-158+107C>G ENSP00000419056.1:n.-158+107C>G
ENST00000473787.5:c.-12+107C>G ENSP00000420274.1:n.-12+107C>G
ENST00000477535.5:c.-12+107C>G ENSP00000419950.1:n.-12+107C>G
ENST00000479582.5:c.-125+107C>G ENSP00000417770.1:n.-125+107C>G
ENST00000488569.5:n.113+107C>G
ENST00000489702.5:c.-12+322C>G ENSP00000418037.1:n.-12+322C>G
ENST00000613821.4:c.-12+107C>G ENSP00000480058.1:n.-12+107C>G
NM_001098629.2:c.-12+107C>G NP_001092099.1:n.-12+107C>G
NM_001098630.2:c.-12+107C>G NP_001092100.1:n.-12+107C>G
NM_001242452.2:c.-12+107C>G NP_001229381.1:n.-12+107C>G
XM_006715974.2:c.-101C>G XP_006716037.1:n.-101C>G
XM_011516160.1:c.-12+322C>G XP_011514462.1:n.-12+322C>G
XM_011516161.1:c.-12+107C>G XP_011514463.1:n.-12+107C>G
XM_011516162.1:c.-12+107C>G XP_011514464.1:n.-12+107C>G
XM_011516164.1:c.-101C>G XP_011514466.1:n.-101C>G
NM_001347928.1:c.-12+891C>G NP_001334857.1:n.-12+891C>G
NM_001098629.3:c.-12+107C>G MANE Select NP_001092099.1:n.-12+107C>G
NM_001098630.3:c.-12+107C>G NP_001092100.1:n.-12+107C>G
NM_001242452.3:c.-12+107C>G NP_001229381.1:n.-12+107C>G
NM_001347928.2:c.-12+891C>G NP_001334857.1:n.-12+891C>G