Canonical Allele Identifier: CA2123848642
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240181C= , CM000676.2:g.24240181C= GRCh38
NC_000014.8:g.24709387C= , CM000676.1:g.24709387C= GRCh37
NC_000014.7:g.23779227C= NCBI36
NG_016650.1:g.7494G=
NG_054634.1:g.12765C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-26G=
ENST00000557921.3:c.*234G= ENSP00000453157.3:n.*234G=
ENST00000699682.1:n.1689G=
ENST00000699683.1:n.1739G=
ENST00000699684.1:c.*892G= ENSP00000514523.1:n.*892G=
ENST00000699685.1:n.1503G=
ENST00000699686.1:c.*234G= ENSP00000514524.1:n.*234G=
ENST00000699687.1:c.*234G= ENSP00000514525.1:n.*234G=
ENST00000699688.1:n.1499G=
ENST00000699689.1:n.1855G=
ENST00000699690.1:n.2052G=
ENST00000699691.1:n.2196G=
ENST00000699692.1:n.71G=
ENST00000699693.1:n.1547-26G=
ENST00000699694.1:n.1958G=
ENST00000699695.1:c.*502-26G= ENSP00000514526.1:n.*502-26G=
ENST00000699696.1:n.1521-26G=
ENST00000699697.1:c.*74G= ENSP00000514527.1:n.*74G=
ENST00000699698.1:n.1132G=
ENST00000699699.1:n.1623G=
ENST00000699700.1:n.1746G=
ENST00000699701.1:c.*679G= ENSP00000514528.1:n.*679G=
ENST00000267415.12:c.1130-26G= MANE Select ENSP00000267415.7:n.1130-26G=
ENST00000646753.1:c.1025-26G= ENSP00000494065.1:n.1025-26G=
ENST00000267415.11:c.1130-26G= ENSP00000267415.7:n.1130-26G=
ENST00000399423.8:c.*234G= ENSP00000382350.4:n.*234G=
ENST00000557915.1:n.337-26G=
ENST00000558566.1:c.*671G= ENSP00000453025.1:n.*671G=
ENST00000558703.1:n.62G=
ENST00000559969.5:c.1057G=
ENST00000560019.5:c.125-26G= ENSP00000453113.1:n.125-26G=
ENST00000626689.2:c.*502-26G= ENSP00000486681.1:n.*502-26G=
NM_001099274.1:c.1130-26G= NP_001092744.1:n.1130-26G=
NM_012461.2:c.*234G= NP_036593.2:n.*234G=
XM_005267528.2:c.1130-26G= XP_005267585.1:n.1130-26G=
XM_005267529.2:c.1025-26G= XP_005267586.1:n.1025-26G=
NM_001099274.2:c.1130-26G= NP_001092744.1:n.1130-26G=
NM_001363668.1:c.1025-26G= NP_001350597.1:n.1025-26G=
NM_012461.3:c.*234G= NP_036593.2:n.*234G=
XM_011536642.2:c.*679G= XP_011534944.1:n.*679G=
XM_017021216.2:c.488-26G= XP_016876705.1:n.488-26G=
XM_017021217.1:c.488-26G= XP_016876706.1:n.488-26G=
NM_001099274.3:c.1130-26G= MANE Select NP_001092744.1:n.1130-26G=
NM_001363668.2:c.1025-26G= NP_001350597.1:n.1025-26G=