Canonical Allele Identifier: CA602355994

Gene: TIRAP

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126290792A>C , CM000673.2:g.126290792A>C	GRCh38
NC_000011.9:g.126160687A>C , CM000673.1:g.126160687A>C	GRCh37
NC_000011.8:g.125665897A>C	NCBI36
NG_011523.1:g.12706A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479770.2:c.-92-11A>C	ENSP00000436967.1:n.-92-11A>C
ENST00000700488.1:c.-92-11A>C	ENSP00000515016.1:n.-92-11A>C
ENST00000700489.1:c.-92-11A>C	ENSP00000515017.1:n.-92-11A>C
ENST00000700490.1:c.-92-11A>C	ENSP00000515018.1:n.-92-11A>C
ENST00000700491.1:c.-92-11A>C	ENSP00000515019.1:n.-92-11A>C
ENST00000700492.1:c.-92-11A>C	ENSP00000515021.1:n.-92-11A>C
ENST00000700493.1:n.1554-11A>C
ENST00000700494.1:n.1164-11A>C
ENST00000700495.1:c.-92-11A>C	ENSP00000515022.1:n.-92-11A>C
ENST00000392679.6:c.-92-11A>C MANE Select	ENSP00000376446.1:n.-92-11A>C
ENST00000392678.7:c.-92-11A>C	ENSP00000376445.3:n.-92-11A>C
ENST00000392679.5:c.-92-11A>C	ENSP00000376446.1:n.-92-11A>C
ENST00000392680.6:c.-92-11A>C	ENSP00000376447.2:n.-92-11A>C
ENST00000462401.1:n.90-11A>C
ENST00000467006.6:n.473-11A>C
ENST00000488598.5:c.-92-11A>C	ENSP00000446213.1:n.-92-11A>C
NM_001039661.1:c.-92-11A>C	NP_001034750.1:n.-92-11A>C
NM_148910.2:c.-92-11A>C	NP_683708.1:n.-92-11A>C
XM_005271399.2:c.236-11A>C	XP_005271456.1:n.236-11A>C
XM_011542576.1:c.-92-11A>C	XP_011540878.1:n.-92-11A>C
XM_011542577.1:c.236-1685A>C	XP_011540879.1:n.236-1685A>C
XM_011542578.1:c.-92-11A>C	XP_011540880.1:n.-92-11A>C
XM_011542579.1:c.-92-11A>C	XP_011540881.1:n.-92-11A>C
XM_011542580.1:c.-92-11A>C	XP_011540882.1:n.-92-11A>C
XM_011542581.1:c.-92-11A>C	XP_011540883.1:n.-92-11A>C
XM_011542582.1:c.-92-11A>C	XP_011540884.1:n.-92-11A>C
NM_001318776.1:c.-92-11A>C	NP_001305705.1:n.-92-11A>C
NM_001318777.1:c.-92-11A>C	NP_001305706.1:n.-92-11A>C
NM_001039661.2:c.-92-11A>C	NP_001034750.1:n.-92-11A>C
NM_001318776.2:c.-92-11A>C	NP_001305705.1:n.-92-11A>C
NM_001318777.2:c.-92-11A>C MANE Select	NP_001305706.1:n.-92-11A>C
NM_148910.3:c.-92-11A>C	NP_683708.1:n.-92-11A>C