Canonical Allele Identifier: CA915223941
Gene: TNIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151078604A>G , CM000667.2:g.151078604A>G GRCh38
NC_000005.9:g.150458165A>G , CM000667.1:g.150458165A>G GRCh37
NC_000005.8:g.150438358A>G NCBI36
NG_030590.1:g.14057T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000521591.6:c.-37+2276T>C MANE Select ENSP00000430760.1:n.-37+2276T>C
ENST00000610535.5:c.-37+2276T>C ENSP00000483944.1:n.-37+2276T>C
ENST00000315050.11:c.-37+8481T>C ENSP00000317891.7:n.-37+8481T>C
ENST00000389378.6:c.-37+2276T>C ENSP00000374029.3:n.-37+2276T>C
ENST00000518977.5:c.-37+2276T>C ENSP00000430971.1:n.-37+2276T>C
ENST00000520695.5:c.-37+1720T>C ENSP00000430279.1:n.-37+1720T>C
ENST00000520931.5:c.-24+2276T>C ENSP00000429891.1:n.-24+2276T>C
ENST00000521001.1:c.-36-13473T>C ENSP00000428404.1:n.-36-13473T>C
ENST00000521591.5:c.-37+2276T>C ENSP00000430760.1:n.-37+2276T>C
ENST00000522100.5:c.-24+8481T>C ENSP00000428487.1:n.-24+8481T>C
ENST00000522226.5:c.-37+8987T>C ENSP00000428187.1:n.-37+8987T>C
ENST00000522926.1:n.424-161T>C
ENST00000523338.5:c.-37+8481T>C ENSP00000428243.1:n.-37+8481T>C
ENST00000610535.4:c.-37+2276T>C ENSP00000483944.1:n.-37+2276T>C
ENST00000610874.4:c.-37+2276T>C ENSP00000484665.1:n.-37+2276T>C
NM_001252385.1:c.-37+2276T>C NP_001239314.1:n.-37+2276T>C
NM_001252386.1:c.-24+2276T>C NP_001239315.1:n.-24+2276T>C
NM_001252390.1:c.-37+8987T>C NP_001239319.1:n.-37+8987T>C
NM_001252391.1:c.-37+8481T>C NP_001239320.1:n.-37+8481T>C
NM_001252392.1:c.-37+8481T>C NP_001239321.1:n.-37+8481T>C
NM_001252393.1:c.-37+2276T>C NP_001239322.1:n.-37+2276T>C
NM_001258454.1:c.-33+2276T>C NP_001245383.1:n.-33+2276T>C
NM_006058.4:c.-37+2276T>C NP_006049.3:n.-37+2276T>C
XM_005268355.1:c.-37+2276T>C XP_005268412.1:n.-37+2276T>C
XM_006714751.1:c.-37+2276T>C XP_006714814.1:n.-37+2276T>C
XM_006714752.1:c.-37+2276T>C XP_006714815.1:n.-37+2276T>C
XM_011537538.1:c.-37+1720T>C XP_011535840.1:n.-37+1720T>C
NM_001364486.1:c.-24+2276T>C NP_001351415.1:n.-24+2276T>C
NM_001364487.1:c.-37+2276T>C NP_001351416.1:n.-37+2276T>C
XM_005268355.2:c.-37+2276T>C XP_005268412.1:n.-37+2276T>C
XM_006714752.3:c.-37+2276T>C XP_006714815.1:n.-37+2276T>C
XM_017008945.2:c.-37+2276T>C XP_016864434.1:n.-37+2276T>C
XM_017008946.2:c.-37+8481T>C XP_016864435.1:n.-37+8481T>C
XM_017008947.2:c.-37+1720T>C XP_016864436.1:n.-37+1720T>C
XM_017008948.2:c.-24+2276T>C XP_016864437.1:n.-24+2276T>C
XM_017008949.2:c.-37+2276T>C XP_016864438.1:n.-37+2276T>C
XM_017008950.2:c.-37+2276T>C XP_016864439.1:n.-37+2276T>C
NM_001252386.2:c.-24+2276T>C NP_001239315.1:n.-24+2276T>C
NM_001252390.2:c.-37+8987T>C NP_001239319.1:n.-37+8987T>C
NM_001252391.2:c.-37+8481T>C NP_001239320.1:n.-37+8481T>C
NM_001252392.2:c.-37+8481T>C NP_001239321.1:n.-37+8481T>C
NM_001252393.2:c.-37+2276T>C NP_001239322.1:n.-37+2276T>C
NM_001258454.2:c.-33+2276T>C NP_001245383.1:n.-33+2276T>C
NM_001364486.2:c.-24+2276T>C NP_001351415.1:n.-24+2276T>C
NM_001364487.2:c.-37+2276T>C NP_001351416.1:n.-37+2276T>C
NM_006058.5:c.-37+2276T>C MANE Select NP_006049.3:n.-37+2276T>C
NM_001252385.2:c.-37+2276T>C NP_001239314.1:n.-37+2276T>C