Canonical Allele Identifier: CA2123848619
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240172A= , CM000676.2:g.24240172A= GRCh38
NC_000014.8:g.24709378A= , CM000676.1:g.24709378A= GRCh37
NC_000014.7:g.23779218A= NCBI36
NG_016650.1:g.7503T=
NG_054634.1:g.12756A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-17T=
ENST00000557921.3:c.*243T= ENSP00000453157.3:n.*243T=
ENST00000699682.1:n.1698T=
ENST00000699683.1:n.1748T=
ENST00000699684.1:c.*901T= ENSP00000514523.1:n.*901T=
ENST00000699685.1:n.1512T=
ENST00000699686.1:c.*243T= ENSP00000514524.1:n.*243T=
ENST00000699687.1:c.*243T= ENSP00000514525.1:n.*243T=
ENST00000699688.1:n.1508T=
ENST00000699689.1:n.1864T=
ENST00000699690.1:n.2061T=
ENST00000699691.1:n.2205T=
ENST00000699692.1:n.80T=
ENST00000699693.1:n.1547-17T=
ENST00000699694.1:n.1967T=
ENST00000699695.1:c.*502-17T= ENSP00000514526.1:n.*502-17T=
ENST00000699696.1:n.1521-17T=
ENST00000699697.1:c.*83T= ENSP00000514527.1:n.*83T=
ENST00000699698.1:n.1141T=
ENST00000699699.1:n.1632T=
ENST00000699700.1:n.1755T=
ENST00000699701.1:c.*688T= ENSP00000514528.1:n.*688T=
ENST00000267415.12:c.1130-17T= MANE Select ENSP00000267415.7:n.1130-17T=
ENST00000646753.1:c.1025-17T= ENSP00000494065.1:n.1025-17T=
ENST00000267415.11:c.1130-17T= ENSP00000267415.7:n.1130-17T=
ENST00000399423.8:c.*243T= ENSP00000382350.4:n.*243T=
ENST00000557915.1:n.337-17T=
ENST00000558566.1:c.*680T= ENSP00000453025.1:n.*680T=
ENST00000558703.1:n.71T=
ENST00000559969.5:c.1066T=
ENST00000560019.5:c.125-17T= ENSP00000453113.1:n.125-17T=
ENST00000626689.2:c.*502-17T= ENSP00000486681.1:n.*502-17T=
NM_001099274.1:c.1130-17T= NP_001092744.1:n.1130-17T=
NM_012461.2:c.*243T= NP_036593.2:n.*243T=
XM_005267528.2:c.1130-17T= XP_005267585.1:n.1130-17T=
XM_005267529.2:c.1025-17T= XP_005267586.1:n.1025-17T=
NM_001099274.2:c.1130-17T= NP_001092744.1:n.1130-17T=
NM_001363668.1:c.1025-17T= NP_001350597.1:n.1025-17T=
NM_012461.3:c.*243T= NP_036593.2:n.*243T=
XM_011536642.2:c.*688T= XP_011534944.1:n.*688T=
XM_017021216.2:c.488-17T= XP_016876705.1:n.488-17T=
XM_017021217.1:c.488-17T= XP_016876706.1:n.488-17T=
NM_001099274.3:c.1130-17T= MANE Select NP_001092744.1:n.1130-17T=
NM_001363668.2:c.1025-17T= NP_001350597.1:n.1025-17T=