Canonical Allele Identifier: CA2007054500
Gene: TIRAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126292764C= , CM000673.2:g.126292764C= GRCh38
NC_000011.9:g.126162659C= , CM000673.1:g.126162659C= GRCh37
NC_000011.8:g.125667869C= NCBI36
NG_011523.1:g.14678C=

Transcript Alleles

HGVS Amino-acid change
ENST00000479770.2:c.355C= ENSP00000436967.1:p.Gln119=
ENST00000700488.1:c.355C= ENSP00000515016.1:p.Gln119=
ENST00000700489.1:c.355C= ENSP00000515017.1:p.Gln119=
ENST00000700490.1:c.355C= ENSP00000515018.1:p.Gln119=
ENST00000700491.1:c.355C= ENSP00000515019.1:p.Gln119=
ENST00000700492.1:c.355C= ENSP00000515021.1:p.Gln119=
ENST00000700493.1:n.2000C=
ENST00000700494.1:n.1610C=
ENST00000700495.1:c.68-904C= ENSP00000515022.1:n.68-904C=
ENST00000700496.1:n.430C=
ENST00000392679.6:c.355C= MANE Select ENSP00000376446.1:p.Gln119=
ENST00000392678.7:c.355C= ENSP00000376445.3:p.Gln119=
ENST00000392679.5:c.355C= ENSP00000376446.1:p.Gln119=
ENST00000392680.6:c.355C= ENSP00000376447.2:p.Gln119=
ENST00000479770.1:c.355C= ENSP00000436967.1:p.Gln119=
NM_001039661.1:c.355C= NP_001034750.1:p.Gln119=
NM_148910.2:c.355C= NP_683708.1:p.Gln119=
XM_005271399.2:c.682C= XP_005271456.1:p.Gln228=
XM_011542576.1:c.355C= XP_011540878.1:p.Gln119=
XM_011542577.1:c.523C= XP_011540879.1:p.Gln175=
XM_011542578.1:c.355C= XP_011540880.1:p.Gln119=
XM_011542579.1:c.355C= XP_011540881.1:p.Gln119=
XM_011542580.1:c.355C= XP_011540882.1:p.Gln119=
XM_011542581.1:c.355C= XP_011540883.1:p.Gln119=
XM_011542582.1:c.355C= XP_011540884.1:p.Gln119=
NM_001318776.1:c.355C= NP_001305705.1:p.Gln119=
NM_001318777.1:c.355C= NP_001305706.1:p.Gln119=
NM_001039661.2:c.355C= NP_001034750.1:p.Gln119=
NM_001318776.2:c.355C= NP_001305705.1:p.Gln119=
NM_001318777.2:c.355C= MANE Select NP_001305706.1:p.Gln119=
NM_148910.3:c.355C= NP_683708.1:p.Gln119=