Canonical Allele Identifier: CA129870625

Gene: TNIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151081138T>C , CM000667.2:g.151081138T>C	GRCh38
NC_000005.9:g.150460699T>C , CM000667.1:g.150460699T>C	GRCh37
NC_000005.8:g.150440892T>C	NCBI36
NG_030590.1:g.11523A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001252390.1:c.-37+6453A>G	NP_001239319.1:n.-37+6453A>G
NM_001252390.2:c.-37+6453A>G	NP_001239319.1:n.-37+6453A>G
NM_001252391.1:c.-37+5947A>G	NP_001239320.1:n.-37+5947A>G
NM_001252391.2:c.-37+5947A>G	NP_001239320.1:n.-37+5947A>G
NM_001252392.1:c.-37+5947A>G	NP_001239321.1:n.-37+5947A>G
NM_001252392.2:c.-37+5947A>G	NP_001239321.1:n.-37+5947A>G
ENST00000315050.11:c.-37+5947A>G	ENSP00000317891.7:n.-37+5947A>G
ENST00000521001.1:c.-37+12300A>G	ENSP00000428404.1:n.-37+12300A>G
ENST00000522100.5:c.-24+5947A>G	ENSP00000428487.1:n.-24+5947A>G
ENST00000522226.5:c.-37+6453A>G	ENSP00000428187.1:n.-37+6453A>G
ENST00000523338.5:c.-37+5947A>G	ENSP00000428243.1:n.-37+5947A>G
XM_011537538.1:c.-331A>G	XP_011535840.1:n.-331A>G
XM_017008946.2:c.-37+5947A>G	XP_016864435.1:n.-37+5947A>G
XM_017008947.2:c.-331A>G	XP_016864436.1:n.-331A>G