Canonical Allele Identifier: CA805649104

Gene: TNIP1

Linked Data

• dbSNP Id: rs1339759463
• gnomAD v3: 5-151060453-C-T
• gnomAD v4: 5-151060453-C-T
• MyVariant Identifiers: chr5:g.150440014C>T (hg19) ; chr5:g.151060453C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151060453C>T , CM000667.2:g.151060453C>T	GRCh38
NC_000005.9:g.150440014C>T , CM000667.1:g.150440014C>T	GRCh37
NC_000005.8:g.150420207C>T	NCBI36
NG_030590.1:g.32208G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000521591.6:c.358-58G>A MANE Select	ENSP00000430760.1:n.358-58G>A
ENST00000610535.5:c.358-58G>A	ENSP00000483944.1:n.358-58G>A
ENST00000315050.11:c.358-58G>A	ENSP00000317891.7:n.358-58G>A
ENST00000389378.6:c.358-58G>A	ENSP00000374029.3:n.358-58G>A
ENST00000518977.5:c.358-58G>A	ENSP00000430971.1:n.358-58G>A
ENST00000519339.5:c.199-58G>A	ENSP00000427854.1:n.199-58G>A
ENST00000520695.5:c.358-58G>A	ENSP00000430279.1:n.358-58G>A
ENST00000520931.5:c.199-58G>A	ENSP00000429891.1:n.199-58G>A
ENST00000521001.1:c.358-58G>A	ENSP00000428404.1:n.358-58G>A
ENST00000521591.5:c.358-58G>A	ENSP00000430760.1:n.358-58G>A
ENST00000522100.5:c.199-58G>A	ENSP00000428487.1:n.199-58G>A
ENST00000522226.5:c.358-58G>A	ENSP00000428187.1:n.358-58G>A
ENST00000523200.5:c.358-58G>A	ENSP00000431105.1:n.358-58G>A
ENST00000523338.5:c.358-58G>A	ENSP00000428243.1:n.358-58G>A
ENST00000524280.5:c.358-58G>A	ENSP00000429912.1:n.358-58G>A
ENST00000610535.4:c.358-58G>A	ENSP00000483944.1:n.358-58G>A
ENST00000610874.4:c.358-58G>A	ENSP00000484665.1:n.358-58G>A
NM_001252385.1:c.358-58G>A	NP_001239314.1:n.358-58G>A
NM_001252386.1:c.199-58G>A	NP_001239315.1:n.199-58G>A
NM_001252390.1:c.358-58G>A	NP_001239319.1:n.358-58G>A
NM_001252391.1:c.358-58G>A	NP_001239320.1:n.358-58G>A
NM_001252392.1:c.358-58G>A	NP_001239321.1:n.358-58G>A
NM_001252393.1:c.358-58G>A	NP_001239322.1:n.358-58G>A
NM_001258454.1:c.358-58G>A	NP_001245383.1:n.358-58G>A
NM_001258455.1:c.358-58G>A	NP_001245384.1:n.358-58G>A
NM_001258456.1:c.358-58G>A	NP_001245385.1:n.358-58G>A
NM_006058.4:c.358-58G>A	NP_006049.3:n.358-58G>A
XM_005268355.1:c.358-58G>A	XP_005268412.1:n.358-58G>A
XM_006714751.1:c.358-58G>A	XP_006714814.1:n.358-58G>A
XM_006714752.1:c.358-58G>A	XP_006714815.1:n.358-58G>A
XM_011537538.1:c.358-58G>A	XP_011535840.1:n.358-58G>A
NM_001364486.1:c.199-58G>A	NP_001351415.1:n.199-58G>A
NM_001364487.1:c.358-58G>A	NP_001351416.1:n.358-58G>A
XM_005268355.2:c.358-58G>A	XP_005268412.1:n.358-58G>A
XM_006714752.3:c.358-58G>A	XP_006714815.1:n.358-58G>A
XM_017008945.2:c.358-58G>A	XP_016864434.1:n.358-58G>A
XM_017008946.2:c.358-58G>A	XP_016864435.1:n.358-58G>A
XM_017008947.2:c.358-58G>A	XP_016864436.1:n.358-58G>A
XM_017008948.2:c.199-58G>A	XP_016864437.1:n.199-58G>A
XM_017008949.2:c.358-58G>A	XP_016864438.1:n.358-58G>A
XM_017008950.2:c.358-58G>A	XP_016864439.1:n.358-58G>A
NM_001252386.2:c.199-58G>A	NP_001239315.1:n.199-58G>A
NM_001252390.2:c.358-58G>A	NP_001239319.1:n.358-58G>A
NM_001252391.2:c.358-58G>A	NP_001239320.1:n.358-58G>A
NM_001252392.2:c.358-58G>A	NP_001239321.1:n.358-58G>A
NM_001252393.2:c.358-58G>A	NP_001239322.1:n.358-58G>A
NM_001258454.2:c.358-58G>A	NP_001245383.1:n.358-58G>A
NM_001364486.2:c.199-58G>A	NP_001351415.1:n.199-58G>A
NM_001364487.2:c.358-58G>A	NP_001351416.1:n.358-58G>A
NM_006058.5:c.358-58G>A MANE Select	NP_006049.3:n.358-58G>A
NM_001252385.2:c.358-58G>A	NP_001239314.1:n.358-58G>A