Canonical Allele Identifier: CA2624345186

Gene: TINF2

Linked Data

• gnomAD v4: 14-24240392-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240392A>T , CM000676.2:g.24240392A>T	GRCh38
NC_000014.8:g.24709598A>T , CM000676.1:g.24709598A>T	GRCh37
NC_000014.7:g.23779438A>T	NCBI36
NG_016650.1:g.7283T>A
NG_054634.1:g.12976A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1391T>A
ENST00000557921.3:c.*23T>A	ENSP00000453157.3:n.*23T>A
ENST00000699682.1:n.1478T>A
ENST00000699683.1:n.1528T>A
ENST00000699684.1:c.*681T>A	ENSP00000514523.1:n.*681T>A
ENST00000699685.1:n.1292T>A
ENST00000699686.1:c.*23T>A	ENSP00000514524.1:n.*23T>A
ENST00000699687.1:c.*23T>A	ENSP00000514525.1:n.*23T>A
ENST00000699688.1:n.1288T>A
ENST00000699689.1:n.1644T>A
ENST00000699690.1:n.1841T>A
ENST00000699691.1:n.1985T>A
ENST00000699693.1:n.1478+27T>A
ENST00000699694.1:n.1747T>A
ENST00000699695.1:c.*433+27T>A	ENSP00000514526.1:n.*433+27T>A
ENST00000699696.1:n.1391T>A
ENST00000699697.1:c.1061+27T>A	ENSP00000514527.1:n.1061+27T>A
ENST00000699698.1:n.982+27T>A
ENST00000699699.1:n.1412T>A
ENST00000699700.1:n.1535T>A
ENST00000699701.1:c.*468T>A	ENSP00000514528.1:n.*468T>A
ENST00000267415.12:c.1061+27T>A MANE Select	ENSP00000267415.7:n.1061+27T>A
ENST00000646753.1:c.956+27T>A	ENSP00000494065.1:n.956+27T>A
ENST00000267415.11:c.1061+27T>A	ENSP00000267415.7:n.1061+27T>A
ENST00000399423.8:c.*23T>A	ENSP00000382350.4:n.*23T>A
ENST00000557915.1:n.207T>A
ENST00000558566.1:c.*460T>A	ENSP00000453025.1:n.*460T>A
ENST00000559969.5:c.846T>A
ENST00000560019.5:c.56+27T>A	ENSP00000453113.1:n.56+27T>A
ENST00000626689.2:c.*433+27T>A	ENSP00000486681.1:n.*433+27T>A
NM_001099274.1:c.1061+27T>A	NP_001092744.1:n.1061+27T>A
NM_012461.2:c.*23T>A	NP_036593.2:n.*23T>A
XM_005267528.2:c.1061+27T>A	XP_005267585.1:n.1061+27T>A
XM_005267529.2:c.956+27T>A	XP_005267586.1:n.956+27T>A
NM_001099274.2:c.1061+27T>A	NP_001092744.1:n.1061+27T>A
NM_001363668.1:c.956+27T>A	NP_001350597.1:n.956+27T>A
NM_012461.3:c.*23T>A	NP_036593.2:n.*23T>A
XM_011536642.2:c.*468T>A	XP_011534944.1:n.*468T>A
XM_017021216.2:c.419+27T>A	XP_016876705.1:n.419+27T>A
XM_017021217.1:c.419+27T>A	XP_016876706.1:n.419+27T>A
NM_001099274.3:c.1061+27T>A MANE Select	NP_001092744.1:n.1061+27T>A
NM_001363668.2:c.956+27T>A	NP_001350597.1:n.956+27T>A