Canonical Allele Identifier: CA2676048745

Gene: TNIP1

Linked Data

• gnomAD v4: 5-151078436-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151078438del , CM000667.2:g.151078438del	GRCh38
NC_000005.9:g.150457999del , CM000667.1:g.150457999del	GRCh37
NC_000005.8:g.150438192del	NCBI36
NG_030590.1:g.14224del

Transcript Alleles

HGVS	Amino-acid change
ENST00000521591.6:c.-37+2443del MANE Select	ENSP00000430760.1:n.-37+2443del
ENST00000610535.5:c.-37+2443del	ENSP00000483944.1:n.-37+2443del
ENST00000315050.11:c.-37+8648del	ENSP00000317891.7:n.-37+8648del
ENST00000389378.6:c.-37+2443del	ENSP00000374029.3:n.-37+2443del
ENST00000518977.5:c.-37+2443del	ENSP00000430971.1:n.-37+2443del
ENST00000520695.5:c.-37+1887del	ENSP00000430279.1:n.-37+1887del
ENST00000520931.5:c.-24+2443del	ENSP00000429891.1:n.-24+2443del
ENST00000521001.1:c.-36-13306del	ENSP00000428404.1:n.-36-13306del
ENST00000521591.5:c.-37+2443del	ENSP00000430760.1:n.-37+2443del
ENST00000522100.5:c.-24+8648del	ENSP00000428487.1:n.-24+8648del
ENST00000522226.5:c.-37+9154del	ENSP00000428187.1:n.-37+9154del
ENST00000522926.1:n.430del
ENST00000523338.5:c.-37+8648del	ENSP00000428243.1:n.-37+8648del
ENST00000610535.4:c.-37+2443del	ENSP00000483944.1:n.-37+2443del
ENST00000610874.4:c.-37+2443del	ENSP00000484665.1:n.-37+2443del
NM_001252385.1:c.-37+2443del	NP_001239314.1:n.-37+2443del
NM_001252386.1:c.-24+2443del	NP_001239315.1:n.-24+2443del
NM_001252390.1:c.-37+9154del	NP_001239319.1:n.-37+9154del
NM_001252391.1:c.-37+8648del	NP_001239320.1:n.-37+8648del
NM_001252392.1:c.-37+8648del	NP_001239321.1:n.-37+8648del
NM_001252393.1:c.-37+2443del	NP_001239322.1:n.-37+2443del
NM_001258454.1:c.-33+2443del	NP_001245383.1:n.-33+2443del
NM_006058.4:c.-37+2443del	NP_006049.3:n.-37+2443del
XM_005268355.1:c.-37+2443del	XP_005268412.1:n.-37+2443del
XM_006714751.1:c.-37+2443del	XP_006714814.1:n.-37+2443del
XM_006714752.1:c.-37+2443del	XP_006714815.1:n.-37+2443del
XM_011537538.1:c.-37+1887del	XP_011535840.1:n.-37+1887del
NM_001364486.1:c.-24+2443del	NP_001351415.1:n.-24+2443del
NM_001364487.1:c.-37+2443del	NP_001351416.1:n.-37+2443del
XM_005268355.2:c.-37+2443del	XP_005268412.1:n.-37+2443del
XM_006714752.3:c.-37+2443del	XP_006714815.1:n.-37+2443del
XM_017008945.2:c.-37+2443del	XP_016864434.1:n.-37+2443del
XM_017008946.2:c.-37+8648del	XP_016864435.1:n.-37+8648del
XM_017008947.2:c.-37+1887del	XP_016864436.1:n.-37+1887del
XM_017008948.2:c.-24+2443del	XP_016864437.1:n.-24+2443del
XM_017008949.2:c.-37+2443del	XP_016864438.1:n.-37+2443del
XM_017008950.2:c.-37+2443del	XP_016864439.1:n.-37+2443del
NM_001252386.2:c.-24+2443del	NP_001239315.1:n.-24+2443del
NM_001252390.2:c.-37+9154del	NP_001239319.1:n.-37+9154del
NM_001252391.2:c.-37+8648del	NP_001239320.1:n.-37+8648del
NM_001252392.2:c.-37+8648del	NP_001239321.1:n.-37+8648del
NM_001252393.2:c.-37+2443del	NP_001239322.1:n.-37+2443del
NM_001258454.2:c.-33+2443del	NP_001245383.1:n.-33+2443del
NM_001364486.2:c.-24+2443del	NP_001351415.1:n.-24+2443del
NM_001364487.2:c.-37+2443del	NP_001351416.1:n.-37+2443del
NM_006058.5:c.-37+2443del MANE Select	NP_006049.3:n.-37+2443del
NM_001252385.2:c.-37+2443del	NP_001239314.1:n.-37+2443del