Canonical Allele Identifier: CA2123849331
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240686C= , CM000676.2:g.24240686C= GRCh38
NC_000014.8:g.24709892C= , CM000676.1:g.24709892C= GRCh37
NC_000014.7:g.23779732C= NCBI36
NG_016650.1:g.6989G=
NG_054634.1:g.13270C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1097G=
ENST00000557921.3:c.686G= ENSP00000453157.3:p.Arg229=
ENST00000699682.1:n.1184G=
ENST00000699683.1:n.1234G=
ENST00000699684.1:c.*387G= ENSP00000514523.1:n.*387G=
ENST00000699685.1:n.998G=
ENST00000699686.1:c.587G= ENSP00000514524.1:p.Arg196=
ENST00000699687.1:c.689G= ENSP00000514525.1:p.Arg230=
ENST00000699688.1:n.994G=
ENST00000699689.1:n.1350G=
ENST00000699690.1:n.1547G=
ENST00000699691.1:n.1691G=
ENST00000699693.1:n.1211G=
ENST00000699694.1:n.1453G=
ENST00000699695.1:c.*166G= ENSP00000514526.1:n.*166G=
ENST00000699696.1:n.1097G=
ENST00000699697.1:c.794G= ENSP00000514527.1:p.Arg265=
ENST00000699698.1:n.715G=
ENST00000699699.1:n.1118G=
ENST00000699700.1:n.1241G=
ENST00000699701.1:c.*174G= ENSP00000514528.1:n.*174G=
ENST00000267415.12:c.794G= MANE Select ENSP00000267415.7:p.Arg265=
ENST00000557921.2:c.686G= ENSP00000453157.2:p.Arg229=
ENST00000646753.1:c.689G= ENSP00000494065.1:p.Arg230=
ENST00000267415.11:c.794G= ENSP00000267415.7:p.Arg265=
ENST00000399423.8:c.794G= ENSP00000382350.4:p.Arg265=
ENST00000558476.5:c.356G= ENSP00000452724.1:p.Arg119=
ENST00000558566.1:c.*166G= ENSP00000453025.1:n.*166G=
ENST00000559019.1:c.*166G= ENSP00000453675.1:n.*166G=
ENST00000559549.1:n.520G=
ENST00000559969.5:c.750G=
ENST00000626689.2:c.*166G= ENSP00000486681.1:n.*166G=
NM_001099274.1:c.794G= NP_001092744.1:p.Arg265=
NM_012461.2:c.794G= NP_036593.2:p.Arg265=
XM_005267528.2:c.794G= XP_005267585.1:p.Arg265=
XM_005267529.2:c.689G= XP_005267586.1:p.Arg230=
NM_001099274.2:c.794G= NP_001092744.1:p.Arg265=
NM_001363668.1:c.689G= NP_001350597.1:p.Arg230=
NM_012461.3:c.794G= NP_036593.2:p.Arg265=
XM_011536642.2:c.*174G= XP_011534944.1:n.*174G=
XM_017021216.2:c.152G= XP_016876705.1:p.Arg51=
XM_017021217.1:c.152G= XP_016876706.1:p.Arg51=
NM_001099274.3:c.794G= MANE Select NP_001092744.1:p.Arg265=
NM_001363668.2:c.689G= NP_001350597.1:p.Arg230=