Canonical Allele Identifier: CA2624345087

Gene: TINF2

Linked Data

• gnomAD v4: 14-24240235-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240235T>C , CM000676.2:g.24240235T>C	GRCh38
NC_000014.8:g.24709441T>C , CM000676.1:g.24709441T>C	GRCh37
NC_000014.7:g.23779281T>C	NCBI36
NG_016650.1:g.7440A>G
NG_054634.1:g.12819T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1520+28A>G
ENST00000557921.3:c.*180A>G	ENSP00000453157.3:n.*180A>G
ENST00000699682.1:n.1635A>G
ENST00000699683.1:n.1685A>G
ENST00000699684.1:c.*838A>G	ENSP00000514523.1:n.*838A>G
ENST00000699685.1:n.1449A>G
ENST00000699686.1:c.*180A>G	ENSP00000514524.1:n.*180A>G
ENST00000699687.1:c.*180A>G	ENSP00000514525.1:n.*180A>G
ENST00000699688.1:n.1445A>G
ENST00000699689.1:n.1801A>G
ENST00000699690.1:n.1998A>G
ENST00000699691.1:n.2142A>G
ENST00000699692.1:n.68+28A>G
ENST00000699693.1:n.1546+28A>G
ENST00000699694.1:n.1904A>G
ENST00000699695.1:c.*501+28A>G	ENSP00000514526.1:n.*501+28A>G
ENST00000699696.1:n.1520+28A>G
ENST00000699697.1:c.*20A>G	ENSP00000514527.1:n.*20A>G
ENST00000699698.1:n.1078A>G
ENST00000699699.1:n.1569A>G
ENST00000699700.1:n.1692A>G
ENST00000699701.1:c.*625A>G	ENSP00000514528.1:n.*625A>G
ENST00000267415.12:c.1129+28A>G MANE Select	ENSP00000267415.7:n.1129+28A>G
ENST00000646753.1:c.1024+28A>G	ENSP00000494065.1:n.1024+28A>G
ENST00000267415.11:c.1129+28A>G	ENSP00000267415.7:n.1129+28A>G
ENST00000399423.8:c.*180A>G	ENSP00000382350.4:n.*180A>G
ENST00000557915.1:n.336+28A>G
ENST00000558566.1:c.*617A>G	ENSP00000453025.1:n.*617A>G
ENST00000558703.1:n.8A>G
ENST00000559969.5:c.1003A>G
ENST00000560019.5:c.124+28A>G	ENSP00000453113.1:n.124+28A>G
ENST00000626689.2:c.*501+28A>G	ENSP00000486681.1:n.*501+28A>G
NM_001099274.1:c.1129+28A>G	NP_001092744.1:n.1129+28A>G
NM_012461.2:c.*180A>G	NP_036593.2:n.*180A>G
XM_005267528.2:c.1129+28A>G	XP_005267585.1:n.1129+28A>G
XM_005267529.2:c.1024+28A>G	XP_005267586.1:n.1024+28A>G
NM_001099274.2:c.1129+28A>G	NP_001092744.1:n.1129+28A>G
NM_001363668.1:c.1024+28A>G	NP_001350597.1:n.1024+28A>G
NM_012461.3:c.*180A>G	NP_036593.2:n.*180A>G
XM_011536642.2:c.*625A>G	XP_011534944.1:n.*625A>G
XM_017021216.2:c.487+28A>G	XP_016876705.1:n.487+28A>G
XM_017021217.1:c.487+28A>G	XP_016876706.1:n.487+28A>G
NM_001099274.3:c.1129+28A>G MANE Select	NP_001092744.1:n.1129+28A>G
NM_001363668.2:c.1024+28A>G	NP_001350597.1:n.1024+28A>G