Canonical Allele Identifier: CA2123848649
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240183A= , CM000676.2:g.24240183A= GRCh38
NC_000014.8:g.24709389A= , CM000676.1:g.24709389A= GRCh37
NC_000014.7:g.23779229A= NCBI36
NG_016650.1:g.7492T=
NG_054634.1:g.12767A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-28T=
ENST00000557921.3:c.*232T= ENSP00000453157.3:n.*232T=
ENST00000699682.1:n.1687T=
ENST00000699683.1:n.1737T=
ENST00000699684.1:c.*890T= ENSP00000514523.1:n.*890T=
ENST00000699685.1:n.1501T=
ENST00000699686.1:c.*232T= ENSP00000514524.1:n.*232T=
ENST00000699687.1:c.*232T= ENSP00000514525.1:n.*232T=
ENST00000699688.1:n.1497T=
ENST00000699689.1:n.1853T=
ENST00000699690.1:n.2050T=
ENST00000699691.1:n.2194T=
ENST00000699692.1:n.69T=
ENST00000699693.1:n.1547-28T=
ENST00000699694.1:n.1956T=
ENST00000699695.1:c.*502-28T= ENSP00000514526.1:n.*502-28T=
ENST00000699696.1:n.1521-28T=
ENST00000699697.1:c.*72T= ENSP00000514527.1:n.*72T=
ENST00000699698.1:n.1130T=
ENST00000699699.1:n.1621T=
ENST00000699700.1:n.1744T=
ENST00000699701.1:c.*677T= ENSP00000514528.1:n.*677T=
ENST00000267415.12:c.1130-28T= MANE Select ENSP00000267415.7:n.1130-28T=
ENST00000646753.1:c.1025-28T= ENSP00000494065.1:n.1025-28T=
ENST00000267415.11:c.1130-28T= ENSP00000267415.7:n.1130-28T=
ENST00000399423.8:c.*232T= ENSP00000382350.4:n.*232T=
ENST00000557915.1:n.337-28T=
ENST00000558566.1:c.*669T= ENSP00000453025.1:n.*669T=
ENST00000558703.1:n.60T=
ENST00000559969.5:c.1055T=
ENST00000560019.5:c.125-28T= ENSP00000453113.1:n.125-28T=
ENST00000626689.2:c.*502-28T= ENSP00000486681.1:n.*502-28T=
NM_001099274.1:c.1130-28T= NP_001092744.1:n.1130-28T=
NM_012461.2:c.*232T= NP_036593.2:n.*232T=
XM_005267528.2:c.1130-28T= XP_005267585.1:n.1130-28T=
XM_005267529.2:c.1025-28T= XP_005267586.1:n.1025-28T=
NM_001099274.2:c.1130-28T= NP_001092744.1:n.1130-28T=
NM_001363668.1:c.1025-28T= NP_001350597.1:n.1025-28T=
NM_012461.3:c.*232T= NP_036593.2:n.*232T=
XM_011536642.2:c.*677T= XP_011534944.1:n.*677T=
XM_017021216.2:c.488-28T= XP_016876705.1:n.488-28T=
XM_017021217.1:c.488-28T= XP_016876706.1:n.488-28T=
NM_001099274.3:c.1130-28T= MANE Select NP_001092744.1:n.1130-28T=
NM_001363668.2:c.1025-28T= NP_001350597.1:n.1025-28T=