Canonical Allele Identifier: CA2123848656
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240184C= , CM000676.2:g.24240184C= GRCh38
NC_000014.8:g.24709390C= , CM000676.1:g.24709390C= GRCh37
NC_000014.7:g.23779230C= NCBI36
NG_016650.1:g.7491G=
NG_054634.1:g.12768C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-29G=
ENST00000557921.3:c.*231G= ENSP00000453157.3:n.*231G=
ENST00000699682.1:n.1686G=
ENST00000699683.1:n.1736G=
ENST00000699684.1:c.*889G= ENSP00000514523.1:n.*889G=
ENST00000699685.1:n.1500G=
ENST00000699686.1:c.*231G= ENSP00000514524.1:n.*231G=
ENST00000699687.1:c.*231G= ENSP00000514525.1:n.*231G=
ENST00000699688.1:n.1496G=
ENST00000699689.1:n.1852G=
ENST00000699690.1:n.2049G=
ENST00000699691.1:n.2193G=
ENST00000699692.1:n.69-1G=
ENST00000699693.1:n.1547-29G=
ENST00000699694.1:n.1955G=
ENST00000699695.1:c.*502-29G= ENSP00000514526.1:n.*502-29G=
ENST00000699696.1:n.1521-29G=
ENST00000699697.1:c.*71G= ENSP00000514527.1:n.*71G=
ENST00000699698.1:n.1129G=
ENST00000699699.1:n.1620G=
ENST00000699700.1:n.1743G=
ENST00000699701.1:c.*676G= ENSP00000514528.1:n.*676G=
ENST00000267415.12:c.1130-29G= MANE Select ENSP00000267415.7:n.1130-29G=
ENST00000646753.1:c.1025-29G= ENSP00000494065.1:n.1025-29G=
ENST00000267415.11:c.1130-29G= ENSP00000267415.7:n.1130-29G=
ENST00000399423.8:c.*231G= ENSP00000382350.4:n.*231G=
ENST00000557915.1:n.337-29G=
ENST00000558566.1:c.*668G= ENSP00000453025.1:n.*668G=
ENST00000558703.1:n.59G=
ENST00000559969.5:c.1054G=
ENST00000560019.5:c.125-29G= ENSP00000453113.1:n.125-29G=
ENST00000626689.2:c.*502-29G= ENSP00000486681.1:n.*502-29G=
NM_001099274.1:c.1130-29G= NP_001092744.1:n.1130-29G=
NM_012461.2:c.*231G= NP_036593.2:n.*231G=
XM_005267528.2:c.1130-29G= XP_005267585.1:n.1130-29G=
XM_005267529.2:c.1025-29G= XP_005267586.1:n.1025-29G=
NM_001099274.2:c.1130-29G= NP_001092744.1:n.1130-29G=
NM_001363668.1:c.1025-29G= NP_001350597.1:n.1025-29G=
NM_012461.3:c.*231G= NP_036593.2:n.*231G=
XM_011536642.2:c.*676G= XP_011534944.1:n.*676G=
XM_017021216.2:c.488-29G= XP_016876705.1:n.488-29G=
XM_017021217.1:c.488-29G= XP_016876706.1:n.488-29G=
NM_001099274.3:c.1130-29G= MANE Select NP_001092744.1:n.1130-29G=
NM_001363668.2:c.1025-29G= NP_001350597.1:n.1025-29G=