Canonical Allele Identifier: CA2007054537

Gene: TIRAP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126292855C= , CM000673.2:g.126292855C=	GRCh38
NC_000011.9:g.126162750C= , CM000673.1:g.126162750C=	GRCh37
NC_000011.8:g.125667960C=	NCBI36
NG_011523.1:g.14769C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000479770.2:c.446C=	ENSP00000436967.1:p.Pro149=
ENST00000700488.1:c.446C=	ENSP00000515016.1:p.Pro149=
ENST00000700489.1:c.446C=	ENSP00000515017.1:p.Pro149=
ENST00000700490.1:c.446C=	ENSP00000515018.1:p.Pro149=
ENST00000700491.1:c.446C=	ENSP00000515019.1:p.Pro149=
ENST00000700492.1:c.446C=	ENSP00000515021.1:p.Pro149=
ENST00000700493.1:n.2091C=
ENST00000700494.1:n.1701C=
ENST00000700495.1:c.68-813C=	ENSP00000515022.1:n.68-813C=
ENST00000700496.1:n.521C=
ENST00000392679.6:c.446C= MANE Select	ENSP00000376446.1:p.Pro149=
ENST00000392678.7:c.446C=	ENSP00000376445.3:p.Pro149=
ENST00000392679.5:c.446C=	ENSP00000376446.1:p.Pro149=
ENST00000392680.6:c.446C=	ENSP00000376447.2:p.Pro149=
ENST00000479770.1:c.446C=	ENSP00000436967.1:p.Pro149=
NM_001039661.1:c.446C=	NP_001034750.1:p.Pro149=
NM_148910.2:c.446C=	NP_683708.1:p.Pro149=
XM_005271399.2:c.773C=	XP_005271456.1:p.Pro258=
XM_011542576.1:c.446C=	XP_011540878.1:p.Pro149=
XM_011542577.1:c.614C=	XP_011540879.1:p.Pro205=
XM_011542578.1:c.446C=	XP_011540880.1:p.Pro149=
XM_011542579.1:c.446C=	XP_011540881.1:p.Pro149=
XM_011542580.1:c.446C=	XP_011540882.1:p.Pro149=
XM_011542581.1:c.446C=	XP_011540883.1:p.Pro149=
XM_011542582.1:c.446C=	XP_011540884.1:p.Pro149=
NM_001318776.1:c.446C=	NP_001305705.1:p.Pro149=
NM_001318777.1:c.446C=	NP_001305706.1:p.Pro149=
NM_001039661.2:c.446C=	NP_001034750.1:p.Pro149=
NM_001318776.2:c.446C=	NP_001305705.1:p.Pro149=
NM_001318777.2:c.446C= MANE Select	NP_001305706.1:p.Pro149=
NM_148910.3:c.446C=	NP_683708.1:p.Pro149=