Canonical Allele Identifier: CA2123848705
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240212G= , CM000676.2:g.24240212G= GRCh38
NC_000014.8:g.24709418G= , CM000676.1:g.24709418G= GRCh37
NC_000014.7:g.23779258G= NCBI36
NG_016650.1:g.7463C=
NG_054634.1:g.12796G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1520+51C=
ENST00000557921.3:c.*203C= ENSP00000453157.3:n.*203C=
ENST00000699682.1:n.1658C=
ENST00000699683.1:n.1708C=
ENST00000699684.1:c.*861C= ENSP00000514523.1:n.*861C=
ENST00000699685.1:n.1472C=
ENST00000699686.1:c.*203C= ENSP00000514524.1:n.*203C=
ENST00000699687.1:c.*203C= ENSP00000514525.1:n.*203C=
ENST00000699688.1:n.1468C=
ENST00000699689.1:n.1824C=
ENST00000699690.1:n.2021C=
ENST00000699691.1:n.2165C=
ENST00000699692.1:n.69-29C=
ENST00000699693.1:n.1546+51C=
ENST00000699694.1:n.1927C=
ENST00000699695.1:c.*501+51C= ENSP00000514526.1:n.*501+51C=
ENST00000699696.1:n.1520+51C=
ENST00000699697.1:c.*43C= ENSP00000514527.1:n.*43C=
ENST00000699698.1:n.1101C=
ENST00000699699.1:n.1592C=
ENST00000699700.1:n.1715C=
ENST00000699701.1:c.*648C= ENSP00000514528.1:n.*648C=
ENST00000267415.12:c.1129+51C= MANE Select ENSP00000267415.7:n.1129+51C=
ENST00000646753.1:c.1024+51C= ENSP00000494065.1:n.1024+51C=
ENST00000267415.11:c.1129+51C= ENSP00000267415.7:n.1129+51C=
ENST00000399423.8:c.*203C= ENSP00000382350.4:n.*203C=
ENST00000557915.1:n.336+51C=
ENST00000558566.1:c.*640C= ENSP00000453025.1:n.*640C=
ENST00000558703.1:n.31C=
ENST00000559969.5:c.1026C=
ENST00000560019.5:c.124+51C= ENSP00000453113.1:n.124+51C=
ENST00000626689.2:c.*501+51C= ENSP00000486681.1:n.*501+51C=
NM_001099274.1:c.1129+51C= NP_001092744.1:n.1129+51C=
NM_012461.2:c.*203C= NP_036593.2:n.*203C=
XM_005267528.2:c.1129+51C= XP_005267585.1:n.1129+51C=
XM_005267529.2:c.1024+51C= XP_005267586.1:n.1024+51C=
NM_001099274.2:c.1129+51C= NP_001092744.1:n.1129+51C=
NM_001363668.1:c.1024+51C= NP_001350597.1:n.1024+51C=
NM_012461.3:c.*203C= NP_036593.2:n.*203C=
XM_011536642.2:c.*648C= XP_011534944.1:n.*648C=
XM_017021216.2:c.487+51C= XP_016876705.1:n.487+51C=
XM_017021217.1:c.487+51C= XP_016876706.1:n.487+51C=
NM_001099274.3:c.1129+51C= MANE Select NP_001092744.1:n.1129+51C=
NM_001363668.2:c.1024+51C= NP_001350597.1:n.1024+51C=