Canonical Allele Identifier: CA805660949

Gene: TNIP1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151081488A>T , CM000667.2:g.151081488A>T	GRCh38
NC_000005.9:g.150461049A>T , CM000667.1:g.150461049A>T	GRCh37
NC_000005.8:g.150441242A>T	NCBI36
NG_030590.1:g.11173T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315050.11:c.-37+5597T>A	ENSP00000317891.7:n.-37+5597T>A
ENST00000521001.1:c.-37+11950T>A	ENSP00000428404.1:n.-37+11950T>A
ENST00000522100.5:c.-24+5597T>A	ENSP00000428487.1:n.-24+5597T>A
ENST00000522226.5:c.-37+6103T>A	ENSP00000428187.1:n.-37+6103T>A
ENST00000523338.5:c.-37+5597T>A	ENSP00000428243.1:n.-37+5597T>A
NM_001252390.1:c.-37+6103T>A	NP_001239319.1:n.-37+6103T>A
NM_001252391.1:c.-37+5597T>A	NP_001239320.1:n.-37+5597T>A
NM_001252392.1:c.-37+5597T>A	NP_001239321.1:n.-37+5597T>A
XM_017008946.2:c.-37+5597T>A	XP_016864435.1:n.-37+5597T>A
XM_017008947.2:c.-681T>A	XP_016864436.1:n.-681T>A
NM_001252390.2:c.-37+6103T>A	NP_001239319.1:n.-37+6103T>A
NM_001252391.2:c.-37+5597T>A	NP_001239320.1:n.-37+5597T>A
NM_001252392.2:c.-37+5597T>A	NP_001239321.1:n.-37+5597T>A