Canonical Allele Identifier: CA2123848681
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240190C= , CM000676.2:g.24240190C= GRCh38
NC_000014.8:g.24709396C= , CM000676.1:g.24709396C= GRCh37
NC_000014.7:g.23779236C= NCBI36
NG_016650.1:g.7485G=
NG_054634.1:g.12774C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-35G=
ENST00000557921.3:c.*225G= ENSP00000453157.3:n.*225G=
ENST00000699682.1:n.1680G=
ENST00000699683.1:n.1730G=
ENST00000699684.1:c.*883G= ENSP00000514523.1:n.*883G=
ENST00000699685.1:n.1494G=
ENST00000699686.1:c.*225G= ENSP00000514524.1:n.*225G=
ENST00000699687.1:c.*225G= ENSP00000514525.1:n.*225G=
ENST00000699688.1:n.1490G=
ENST00000699689.1:n.1846G=
ENST00000699690.1:n.2043G=
ENST00000699691.1:n.2187G=
ENST00000699692.1:n.69-7G=
ENST00000699693.1:n.1547-35G=
ENST00000699694.1:n.1949G=
ENST00000699695.1:c.*502-35G= ENSP00000514526.1:n.*502-35G=
ENST00000699696.1:n.1521-35G=
ENST00000699697.1:c.*65G= ENSP00000514527.1:n.*65G=
ENST00000699698.1:n.1123G=
ENST00000699699.1:n.1614G=
ENST00000699700.1:n.1737G=
ENST00000699701.1:c.*670G= ENSP00000514528.1:n.*670G=
ENST00000267415.12:c.1130-35G= MANE Select ENSP00000267415.7:n.1130-35G=
ENST00000646753.1:c.1025-35G= ENSP00000494065.1:n.1025-35G=
ENST00000267415.11:c.1130-35G= ENSP00000267415.7:n.1130-35G=
ENST00000399423.8:c.*225G= ENSP00000382350.4:n.*225G=
ENST00000557915.1:n.337-35G=
ENST00000558566.1:c.*662G= ENSP00000453025.1:n.*662G=
ENST00000558703.1:n.53G=
ENST00000559969.5:c.1048G=
ENST00000560019.5:c.125-35G= ENSP00000453113.1:n.125-35G=
ENST00000626689.2:c.*502-35G= ENSP00000486681.1:n.*502-35G=
NM_001099274.1:c.1130-35G= NP_001092744.1:n.1130-35G=
NM_012461.2:c.*225G= NP_036593.2:n.*225G=
XM_005267528.2:c.1130-35G= XP_005267585.1:n.1130-35G=
XM_005267529.2:c.1025-35G= XP_005267586.1:n.1025-35G=
NM_001099274.2:c.1130-35G= NP_001092744.1:n.1130-35G=
NM_001363668.1:c.1025-35G= NP_001350597.1:n.1025-35G=
NM_012461.3:c.*225G= NP_036593.2:n.*225G=
XM_011536642.2:c.*670G= XP_011534944.1:n.*670G=
XM_017021216.2:c.488-35G= XP_016876705.1:n.488-35G=
XM_017021217.1:c.488-35G= XP_016876706.1:n.488-35G=
NM_001099274.3:c.1130-35G= MANE Select NP_001092744.1:n.1130-35G=
NM_001363668.2:c.1025-35G= NP_001350597.1:n.1025-35G=