Canonical Allele Identifier: CA2123849330
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240684G= , CM000676.2:g.24240684G= GRCh38
NC_000014.8:g.24709890G= , CM000676.1:g.24709890G= GRCh37
NC_000014.7:g.23779730G= NCBI36
NG_016650.1:g.6991C=
NG_054634.1:g.13268G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1099C=
ENST00000557921.3:c.688C= ENSP00000453157.3:p.Arg230=
ENST00000699682.1:n.1186C=
ENST00000699683.1:n.1236C=
ENST00000699684.1:c.*389C= ENSP00000514523.1:n.*389C=
ENST00000699685.1:n.1000C=
ENST00000699686.1:c.589C= ENSP00000514524.1:p.Arg197=
ENST00000699687.1:c.691C= ENSP00000514525.1:p.Arg231=
ENST00000699688.1:n.996C=
ENST00000699689.1:n.1352C=
ENST00000699690.1:n.1549C=
ENST00000699691.1:n.1693C=
ENST00000699693.1:n.1213C=
ENST00000699694.1:n.1455C=
ENST00000699695.1:c.*168C= ENSP00000514526.1:n.*168C=
ENST00000699696.1:n.1099C=
ENST00000699697.1:c.796C= ENSP00000514527.1:p.Arg266=
ENST00000699698.1:n.717C=
ENST00000699699.1:n.1120C=
ENST00000699700.1:n.1243C=
ENST00000699701.1:c.*176C= ENSP00000514528.1:n.*176C=
ENST00000267415.12:c.796C= MANE Select ENSP00000267415.7:p.Arg266=
ENST00000557921.2:c.688C= ENSP00000453157.2:p.Arg230=
ENST00000646753.1:c.691C= ENSP00000494065.1:p.Arg231=
ENST00000267415.11:c.796C= ENSP00000267415.7:p.Arg266=
ENST00000399423.8:c.796C= ENSP00000382350.4:p.Arg266=
ENST00000558476.5:c.358C= ENSP00000452724.1:p.Arg120=
ENST00000558566.1:c.*168C= ENSP00000453025.1:n.*168C=
ENST00000559019.1:c.*168C= ENSP00000453675.1:n.*168C=
ENST00000559549.1:n.522C=
ENST00000559969.5:c.752C=
ENST00000626689.2:c.*168C= ENSP00000486681.1:n.*168C=
NM_001099274.1:c.796C= NP_001092744.1:p.Arg266=
NM_012461.2:c.796C= NP_036593.2:p.Arg266=
XM_005267528.2:c.796C= XP_005267585.1:p.Arg266=
XM_005267529.2:c.691C= XP_005267586.1:p.Arg231=
NM_001099274.2:c.796C= NP_001092744.1:p.Arg266=
NM_001363668.1:c.691C= NP_001350597.1:p.Arg231=
NM_012461.3:c.796C= NP_036593.2:p.Arg266=
XM_011536642.2:c.*176C= XP_011534944.1:n.*176C=
XM_017021216.2:c.154C= XP_016876705.1:p.Arg52=
XM_017021217.1:c.154C= XP_016876706.1:p.Arg52=
NM_001099274.3:c.796C= MANE Select NP_001092744.1:p.Arg266=
NM_001363668.2:c.691C= NP_001350597.1:p.Arg231=