Canonical Allele Identifier: CA1591227403
Gene: TNIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151070730T= , CM000667.2:g.151070730T= GRCh38
NC_000005.9:g.150450291T= , CM000667.1:g.150450291T= GRCh37
NC_000005.8:g.150430484T= NCBI36
NG_030590.1:g.21931A=

Transcript Alleles

HGVS Amino-acid change
ENST00000521591.6:c.-36-5599A= MANE Select ENSP00000430760.1:n.-36-5599A=
ENST00000610535.5:c.-36-5599A= ENSP00000483944.1:n.-36-5599A=
ENST00000315050.11:c.-36-5599A= ENSP00000317891.7:n.-36-5599A=
ENST00000389378.6:c.-36-5599A= ENSP00000374029.3:n.-36-5599A=
ENST00000518977.5:c.-36-5599A= ENSP00000430971.1:n.-36-5599A=
ENST00000520695.5:c.-36-5599A= ENSP00000430279.1:n.-36-5599A=
ENST00000520931.5:c.-23-6983A= ENSP00000429891.1:n.-23-6983A=
ENST00000521001.1:c.-36-5599A= ENSP00000428404.1:n.-36-5599A=
ENST00000521591.5:c.-36-5599A= ENSP00000430760.1:n.-36-5599A=
ENST00000522100.5:c.-23-6983A= ENSP00000428487.1:n.-23-6983A=
ENST00000522226.5:c.-36-5599A= ENSP00000428187.1:n.-36-5599A=
ENST00000523338.5:c.-36-5599A= ENSP00000428243.1:n.-36-5599A=
ENST00000610535.4:c.-36-5599A= ENSP00000483944.1:n.-36-5599A=
ENST00000610874.4:c.-36-5599A= ENSP00000484665.1:n.-36-5599A=
NM_001252385.1:c.-36-5599A= NP_001239314.1:n.-36-5599A=
NM_001252386.1:c.-23-6983A= NP_001239315.1:n.-23-6983A=
NM_001252390.1:c.-36-5599A= NP_001239319.1:n.-36-5599A=
NM_001252391.1:c.-36-5599A= NP_001239320.1:n.-36-5599A=
NM_001252392.1:c.-36-5599A= NP_001239321.1:n.-36-5599A=
NM_001252393.1:c.-36-5599A= NP_001239322.1:n.-36-5599A=
NM_001258454.1:c.-32-5603A= NP_001245383.1:n.-32-5603A=
NM_006058.4:c.-36-5599A= NP_006049.3:n.-36-5599A=
XM_005268355.1:c.-36-5599A= XP_005268412.1:n.-36-5599A=
XM_006714751.1:c.-36-5599A= XP_006714814.1:n.-36-5599A=
XM_006714752.1:c.-36-5599A= XP_006714815.1:n.-36-5599A=
XM_011537538.1:c.-36-5599A= XP_011535840.1:n.-36-5599A=
NM_001364486.1:c.-23-6983A= NP_001351415.1:n.-23-6983A=
NM_001364487.1:c.-36-5599A= NP_001351416.1:n.-36-5599A=
XM_005268355.2:c.-36-5599A= XP_005268412.1:n.-36-5599A=
XM_006714752.3:c.-36-5599A= XP_006714815.1:n.-36-5599A=
XM_017008945.2:c.-36-5599A= XP_016864434.1:n.-36-5599A=
XM_017008946.2:c.-36-5599A= XP_016864435.1:n.-36-5599A=
XM_017008947.2:c.-36-5599A= XP_016864436.1:n.-36-5599A=
XM_017008948.2:c.-23-6983A= XP_016864437.1:n.-23-6983A=
XM_017008949.2:c.-36-5599A= XP_016864438.1:n.-36-5599A=
XM_017008950.2:c.-36-5599A= XP_016864439.1:n.-36-5599A=
NM_001252386.2:c.-23-6983A= NP_001239315.1:n.-23-6983A=
NM_001252390.2:c.-36-5599A= NP_001239319.1:n.-36-5599A=
NM_001252391.2:c.-36-5599A= NP_001239320.1:n.-36-5599A=
NM_001252392.2:c.-36-5599A= NP_001239321.1:n.-36-5599A=
NM_001252393.2:c.-36-5599A= NP_001239322.1:n.-36-5599A=
NM_001258454.2:c.-32-5603A= NP_001245383.1:n.-32-5603A=
NM_001364486.2:c.-23-6983A= NP_001351415.1:n.-23-6983A=
NM_001364487.2:c.-36-5599A= NP_001351416.1:n.-36-5599A=
NM_006058.5:c.-36-5599A= MANE Select NP_006049.3:n.-36-5599A=
NM_001252385.2:c.-36-5599A= NP_001239314.1:n.-36-5599A=