Canonical Allele Identifier: CA2123848679
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240189T= , CM000676.2:g.24240189T= GRCh38
NC_000014.8:g.24709395T= , CM000676.1:g.24709395T= GRCh37
NC_000014.7:g.23779235T= NCBI36
NG_016650.1:g.7486A=
NG_054634.1:g.12773T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-34A=
ENST00000557921.3:c.*226A= ENSP00000453157.3:n.*226A=
ENST00000699682.1:n.1681A=
ENST00000699683.1:n.1731A=
ENST00000699684.1:c.*884A= ENSP00000514523.1:n.*884A=
ENST00000699685.1:n.1495A=
ENST00000699686.1:c.*226A= ENSP00000514524.1:n.*226A=
ENST00000699687.1:c.*226A= ENSP00000514525.1:n.*226A=
ENST00000699688.1:n.1491A=
ENST00000699689.1:n.1847A=
ENST00000699690.1:n.2044A=
ENST00000699691.1:n.2188A=
ENST00000699692.1:n.69-6A=
ENST00000699693.1:n.1547-34A=
ENST00000699694.1:n.1950A=
ENST00000699695.1:c.*502-34A= ENSP00000514526.1:n.*502-34A=
ENST00000699696.1:n.1521-34A=
ENST00000699697.1:c.*66A= ENSP00000514527.1:n.*66A=
ENST00000699698.1:n.1124A=
ENST00000699699.1:n.1615A=
ENST00000699700.1:n.1738A=
ENST00000699701.1:c.*671A= ENSP00000514528.1:n.*671A=
ENST00000267415.12:c.1130-34A= MANE Select ENSP00000267415.7:n.1130-34A=
ENST00000646753.1:c.1025-34A= ENSP00000494065.1:n.1025-34A=
ENST00000267415.11:c.1130-34A= ENSP00000267415.7:n.1130-34A=
ENST00000399423.8:c.*226A= ENSP00000382350.4:n.*226A=
ENST00000557915.1:n.337-34A=
ENST00000558566.1:c.*663A= ENSP00000453025.1:n.*663A=
ENST00000558703.1:n.54A=
ENST00000559969.5:c.1049A=
ENST00000560019.5:c.125-34A= ENSP00000453113.1:n.125-34A=
ENST00000626689.2:c.*502-34A= ENSP00000486681.1:n.*502-34A=
NM_001099274.1:c.1130-34A= NP_001092744.1:n.1130-34A=
NM_012461.2:c.*226A= NP_036593.2:n.*226A=
XM_005267528.2:c.1130-34A= XP_005267585.1:n.1130-34A=
XM_005267529.2:c.1025-34A= XP_005267586.1:n.1025-34A=
NM_001099274.2:c.1130-34A= NP_001092744.1:n.1130-34A=
NM_001363668.1:c.1025-34A= NP_001350597.1:n.1025-34A=
NM_012461.3:c.*226A= NP_036593.2:n.*226A=
XM_011536642.2:c.*671A= XP_011534944.1:n.*671A=
XM_017021216.2:c.488-34A= XP_016876705.1:n.488-34A=
XM_017021217.1:c.488-34A= XP_016876706.1:n.488-34A=
NM_001099274.3:c.1130-34A= MANE Select NP_001092744.1:n.1130-34A=
NM_001363668.2:c.1025-34A= NP_001350597.1:n.1025-34A=