Canonical Allele Identifier: CA2123849233
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240507T= , CM000676.2:g.24240507T= GRCh38
NC_000014.8:g.24709713T= , CM000676.1:g.24709713T= GRCh37
NC_000014.7:g.23779553T= NCBI36
NG_016650.1:g.7168A=
NG_054634.1:g.13091T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1276A=
ENST00000557921.3:c.865A= ENSP00000453157.3:p.Thr289=
ENST00000699682.1:n.1363A=
ENST00000699683.1:n.1413A=
ENST00000699684.1:c.*566A= ENSP00000514523.1:n.*566A=
ENST00000699685.1:n.1177A=
ENST00000699686.1:c.766A= ENSP00000514524.1:p.Thr256=
ENST00000699687.1:c.868A= ENSP00000514525.1:p.Thr290=
ENST00000699688.1:n.1173A=
ENST00000699689.1:n.1529A=
ENST00000699690.1:n.1726A=
ENST00000699691.1:n.1870A=
ENST00000699693.1:n.1390A=
ENST00000699694.1:n.1632A=
ENST00000699695.1:c.*345A= ENSP00000514526.1:n.*345A=
ENST00000699696.1:n.1276A=
ENST00000699697.1:c.973A= ENSP00000514527.1:p.Thr325=
ENST00000699698.1:n.894A=
ENST00000699699.1:n.1297A=
ENST00000699700.1:n.1420A=
ENST00000699701.1:c.*353A= ENSP00000514528.1:n.*353A=
ENST00000267415.12:c.973A= MANE Select ENSP00000267415.7:p.Thr325=
ENST00000557921.2:c.865A= ENSP00000453157.2:p.Thr289=
ENST00000646753.1:c.868A= ENSP00000494065.1:p.Thr290=
ENST00000267415.11:c.973A= ENSP00000267415.7:p.Thr325=
ENST00000399423.8:c.973A= ENSP00000382350.4:p.Thr325=
ENST00000557915.1:n.92A=
ENST00000558566.1:c.*345A= ENSP00000453025.1:n.*345A=
ENST00000559019.1:c.*345A= ENSP00000453675.1:n.*345A=
ENST00000559969.5:c.758-27A=
ENST00000626689.2:c.*345A= ENSP00000486681.1:n.*345A=
NM_001099274.1:c.973A= NP_001092744.1:p.Thr325=
NM_012461.2:c.973A= NP_036593.2:p.Thr325=
XM_005267528.2:c.973A= XP_005267585.1:p.Thr325=
XM_005267529.2:c.868A= XP_005267586.1:p.Thr290=
NM_001099274.2:c.973A= NP_001092744.1:p.Thr325=
NM_001363668.1:c.868A= NP_001350597.1:p.Thr290=
NM_012461.3:c.973A= NP_036593.2:p.Thr325=
XM_011536642.2:c.*353A= XP_011534944.1:n.*353A=
XM_017021216.2:c.331A= XP_016876705.1:p.Thr111=
XM_017021217.1:c.331A= XP_016876706.1:p.Thr111=
NM_001099274.3:c.973A= MANE Select NP_001092744.1:p.Thr325=
NM_001363668.2:c.868A= NP_001350597.1:p.Thr290=