Canonical Allele Identifier: CA2123848632
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240178A= , CM000676.2:g.24240178A= GRCh38
NC_000014.8:g.24709384A= , CM000676.1:g.24709384A= GRCh37
NC_000014.7:g.23779224A= NCBI36
NG_016650.1:g.7497T=
NG_054634.1:g.12762A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-23T=
ENST00000557921.3:c.*237T= ENSP00000453157.3:n.*237T=
ENST00000699682.1:n.1692T=
ENST00000699683.1:n.1742T=
ENST00000699684.1:c.*895T= ENSP00000514523.1:n.*895T=
ENST00000699685.1:n.1506T=
ENST00000699686.1:c.*237T= ENSP00000514524.1:n.*237T=
ENST00000699687.1:c.*237T= ENSP00000514525.1:n.*237T=
ENST00000699688.1:n.1502T=
ENST00000699689.1:n.1858T=
ENST00000699690.1:n.2055T=
ENST00000699691.1:n.2199T=
ENST00000699692.1:n.74T=
ENST00000699693.1:n.1547-23T=
ENST00000699694.1:n.1961T=
ENST00000699695.1:c.*502-23T= ENSP00000514526.1:n.*502-23T=
ENST00000699696.1:n.1521-23T=
ENST00000699697.1:c.*77T= ENSP00000514527.1:n.*77T=
ENST00000699698.1:n.1135T=
ENST00000699699.1:n.1626T=
ENST00000699700.1:n.1749T=
ENST00000699701.1:c.*682T= ENSP00000514528.1:n.*682T=
ENST00000267415.12:c.1130-23T= MANE Select ENSP00000267415.7:n.1130-23T=
ENST00000646753.1:c.1025-23T= ENSP00000494065.1:n.1025-23T=
ENST00000267415.11:c.1130-23T= ENSP00000267415.7:n.1130-23T=
ENST00000399423.8:c.*237T= ENSP00000382350.4:n.*237T=
ENST00000557915.1:n.337-23T=
ENST00000558566.1:c.*674T= ENSP00000453025.1:n.*674T=
ENST00000558703.1:n.65T=
ENST00000559969.5:c.1060T=
ENST00000560019.5:c.125-23T= ENSP00000453113.1:n.125-23T=
ENST00000626689.2:c.*502-23T= ENSP00000486681.1:n.*502-23T=
NM_001099274.1:c.1130-23T= NP_001092744.1:n.1130-23T=
NM_012461.2:c.*237T= NP_036593.2:n.*237T=
XM_005267528.2:c.1130-23T= XP_005267585.1:n.1130-23T=
XM_005267529.2:c.1025-23T= XP_005267586.1:n.1025-23T=
NM_001099274.2:c.1130-23T= NP_001092744.1:n.1130-23T=
NM_001363668.1:c.1025-23T= NP_001350597.1:n.1025-23T=
NM_012461.3:c.*237T= NP_036593.2:n.*237T=
XM_011536642.2:c.*682T= XP_011534944.1:n.*682T=
XM_017021216.2:c.488-23T= XP_016876705.1:n.488-23T=
XM_017021217.1:c.488-23T= XP_016876706.1:n.488-23T=
NM_001099274.3:c.1130-23T= MANE Select NP_001092744.1:n.1130-23T=
NM_001363668.2:c.1025-23T= NP_001350597.1:n.1025-23T=