Canonical Allele Identifier: CA2123848774
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240255C= , CM000676.2:g.24240255C= GRCh38
NC_000014.8:g.24709461C= , CM000676.1:g.24709461C= GRCh37
NC_000014.7:g.23779301C= NCBI36
NG_016650.1:g.7420G=
NG_054634.1:g.12839C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1520+8G=
ENST00000557921.3:c.*160G= ENSP00000453157.3:n.*160G=
ENST00000699682.1:n.1615G=
ENST00000699683.1:n.1665G=
ENST00000699684.1:c.*818G= ENSP00000514523.1:n.*818G=
ENST00000699685.1:n.1429G=
ENST00000699686.1:c.*160G= ENSP00000514524.1:n.*160G=
ENST00000699687.1:c.*160G= ENSP00000514525.1:n.*160G=
ENST00000699688.1:n.1425G=
ENST00000699689.1:n.1781G=
ENST00000699690.1:n.1978G=
ENST00000699691.1:n.2122G=
ENST00000699692.1:n.68+8G=
ENST00000699693.1:n.1546+8G=
ENST00000699694.1:n.1884G=
ENST00000699695.1:c.*501+8G= ENSP00000514526.1:n.*501+8G=
ENST00000699696.1:n.1520+8G=
ENST00000699697.1:c.1137G= ENSP00000514527.1:p.Ter379=
ENST00000699698.1:n.1058G=
ENST00000699699.1:n.1549G=
ENST00000699700.1:n.1672G=
ENST00000699701.1:c.*605G= ENSP00000514528.1:n.*605G=
ENST00000267415.12:c.1129+8G= MANE Select ENSP00000267415.7:n.1129+8G=
ENST00000646753.1:c.1024+8G= ENSP00000494065.1:n.1024+8G=
ENST00000267415.11:c.1129+8G= ENSP00000267415.7:n.1129+8G=
ENST00000399423.8:c.*160G= ENSP00000382350.4:n.*160G=
ENST00000557915.1:n.336+8G=
ENST00000558566.1:c.*597G= ENSP00000453025.1:n.*597G=
ENST00000559969.5:c.983G=
ENST00000560019.5:c.124+8G= ENSP00000453113.1:n.124+8G=
ENST00000626689.2:c.*501+8G= ENSP00000486681.1:n.*501+8G=
NM_001099274.1:c.1129+8G= NP_001092744.1:n.1129+8G=
NM_012461.2:c.*160G= NP_036593.2:n.*160G=
XM_005267528.2:c.1129+8G= XP_005267585.1:n.1129+8G=
XM_005267529.2:c.1024+8G= XP_005267586.1:n.1024+8G=
NM_001099274.2:c.1129+8G= NP_001092744.1:n.1129+8G=
NM_001363668.1:c.1024+8G= NP_001350597.1:n.1024+8G=
NM_012461.3:c.*160G= NP_036593.2:n.*160G=
XM_011536642.2:c.*605G= XP_011534944.1:n.*605G=
XM_017021216.2:c.487+8G= XP_016876705.1:n.487+8G=
XM_017021217.1:c.487+8G= XP_016876706.1:n.487+8G=
NM_001099274.3:c.1129+8G= MANE Select NP_001092744.1:n.1129+8G=
NM_001363668.2:c.1024+8G= NP_001350597.1:n.1024+8G=