Canonical Allele Identifier: CA2007054499
Gene: TIRAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126292763G= , CM000673.2:g.126292763G= GRCh38
NC_000011.9:g.126162658G= , CM000673.1:g.126162658G= GRCh37
NC_000011.8:g.125667868G= NCBI36
NG_011523.1:g.14677G=

Transcript Alleles

HGVS Amino-acid change
ENST00000479770.2:c.354G= ENSP00000436967.1:p.Leu118=
ENST00000700488.1:c.354G= ENSP00000515016.1:p.Leu118=
ENST00000700489.1:c.354G= ENSP00000515017.1:p.Leu118=
ENST00000700490.1:c.354G= ENSP00000515018.1:p.Leu118=
ENST00000700491.1:c.354G= ENSP00000515019.1:p.Leu118=
ENST00000700492.1:c.354G= ENSP00000515021.1:p.Leu118=
ENST00000700493.1:n.1999G=
ENST00000700494.1:n.1609G=
ENST00000700495.1:c.68-905G= ENSP00000515022.1:n.68-905G=
ENST00000700496.1:n.429G=
ENST00000392679.6:c.354G= MANE Select ENSP00000376446.1:p.Leu118=
ENST00000392678.7:c.354G= ENSP00000376445.3:p.Leu118=
ENST00000392679.5:c.354G= ENSP00000376446.1:p.Leu118=
ENST00000392680.6:c.354G= ENSP00000376447.2:p.Leu118=
ENST00000479770.1:c.354G= ENSP00000436967.1:p.Leu118=
NM_001039661.1:c.354G= NP_001034750.1:p.Leu118=
NM_148910.2:c.354G= NP_683708.1:p.Leu118=
XM_005271399.2:c.681G= XP_005271456.1:p.Leu227=
XM_011542576.1:c.354G= XP_011540878.1:p.Leu118=
XM_011542577.1:c.522G= XP_011540879.1:p.Leu174=
XM_011542578.1:c.354G= XP_011540880.1:p.Leu118=
XM_011542579.1:c.354G= XP_011540881.1:p.Leu118=
XM_011542580.1:c.354G= XP_011540882.1:p.Leu118=
XM_011542581.1:c.354G= XP_011540883.1:p.Leu118=
XM_011542582.1:c.354G= XP_011540884.1:p.Leu118=
NM_001318776.1:c.354G= NP_001305705.1:p.Leu118=
NM_001318777.1:c.354G= NP_001305706.1:p.Leu118=
NM_001039661.2:c.354G= NP_001034750.1:p.Leu118=
NM_001318776.2:c.354G= NP_001305705.1:p.Leu118=
NM_001318777.2:c.354G= MANE Select NP_001305706.1:p.Leu118=
NM_148910.3:c.354G= NP_683708.1:p.Leu118=