Canonical Allele Identifier: CA2123848625
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240173G= , CM000676.2:g.24240173G= GRCh38
NC_000014.8:g.24709379G= , CM000676.1:g.24709379G= GRCh37
NC_000014.7:g.23779219G= NCBI36
NG_016650.1:g.7502C=
NG_054634.1:g.12757G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1521-18C=
ENST00000557921.3:c.*242C= ENSP00000453157.3:n.*242C=
ENST00000699682.1:n.1697C=
ENST00000699683.1:n.1747C=
ENST00000699684.1:c.*900C= ENSP00000514523.1:n.*900C=
ENST00000699685.1:n.1511C=
ENST00000699686.1:c.*242C= ENSP00000514524.1:n.*242C=
ENST00000699687.1:c.*242C= ENSP00000514525.1:n.*242C=
ENST00000699688.1:n.1507C=
ENST00000699689.1:n.1863C=
ENST00000699690.1:n.2060C=
ENST00000699691.1:n.2204C=
ENST00000699692.1:n.79C=
ENST00000699693.1:n.1547-18C=
ENST00000699694.1:n.1966C=
ENST00000699695.1:c.*502-18C= ENSP00000514526.1:n.*502-18C=
ENST00000699696.1:n.1521-18C=
ENST00000699697.1:c.*82C= ENSP00000514527.1:n.*82C=
ENST00000699698.1:n.1140C=
ENST00000699699.1:n.1631C=
ENST00000699700.1:n.1754C=
ENST00000699701.1:c.*687C= ENSP00000514528.1:n.*687C=
ENST00000267415.12:c.1130-18C= MANE Select ENSP00000267415.7:n.1130-18C=
ENST00000646753.1:c.1025-18C= ENSP00000494065.1:n.1025-18C=
ENST00000267415.11:c.1130-18C= ENSP00000267415.7:n.1130-18C=
ENST00000399423.8:c.*242C= ENSP00000382350.4:n.*242C=
ENST00000557915.1:n.337-18C=
ENST00000558566.1:c.*679C= ENSP00000453025.1:n.*679C=
ENST00000558703.1:n.70C=
ENST00000559969.5:c.1065C=
ENST00000560019.5:c.125-18C= ENSP00000453113.1:n.125-18C=
ENST00000626689.2:c.*502-18C= ENSP00000486681.1:n.*502-18C=
NM_001099274.1:c.1130-18C= NP_001092744.1:n.1130-18C=
NM_012461.2:c.*242C= NP_036593.2:n.*242C=
XM_005267528.2:c.1130-18C= XP_005267585.1:n.1130-18C=
XM_005267529.2:c.1025-18C= XP_005267586.1:n.1025-18C=
NM_001099274.2:c.1130-18C= NP_001092744.1:n.1130-18C=
NM_001363668.1:c.1025-18C= NP_001350597.1:n.1025-18C=
NM_012461.3:c.*242C= NP_036593.2:n.*242C=
XM_011536642.2:c.*687C= XP_011534944.1:n.*687C=
XM_017021216.2:c.488-18C= XP_016876705.1:n.488-18C=
XM_017021217.1:c.488-18C= XP_016876706.1:n.488-18C=
NM_001099274.3:c.1130-18C= MANE Select NP_001092744.1:n.1130-18C=
NM_001363668.2:c.1025-18C= NP_001350597.1:n.1025-18C=