Canonical Allele Identifier: CA2123848729
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240225A= , CM000676.2:g.24240225A= GRCh38
NC_000014.8:g.24709431A= , CM000676.1:g.24709431A= GRCh37
NC_000014.7:g.23779271A= NCBI36
NG_016650.1:g.7450T=
NG_054634.1:g.12809A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1520+38T=
ENST00000557921.3:c.*190T= ENSP00000453157.3:n.*190T=
ENST00000699682.1:n.1645T=
ENST00000699683.1:n.1695T=
ENST00000699684.1:c.*848T= ENSP00000514523.1:n.*848T=
ENST00000699685.1:n.1459T=
ENST00000699686.1:c.*190T= ENSP00000514524.1:n.*190T=
ENST00000699687.1:c.*190T= ENSP00000514525.1:n.*190T=
ENST00000699688.1:n.1455T=
ENST00000699689.1:n.1811T=
ENST00000699690.1:n.2008T=
ENST00000699691.1:n.2152T=
ENST00000699692.1:n.68+38T=
ENST00000699693.1:n.1546+38T=
ENST00000699694.1:n.1914T=
ENST00000699695.1:c.*501+38T= ENSP00000514526.1:n.*501+38T=
ENST00000699696.1:n.1520+38T=
ENST00000699697.1:c.*30T= ENSP00000514527.1:n.*30T=
ENST00000699698.1:n.1088T=
ENST00000699699.1:n.1579T=
ENST00000699700.1:n.1702T=
ENST00000699701.1:c.*635T= ENSP00000514528.1:n.*635T=
ENST00000267415.12:c.1129+38T= MANE Select ENSP00000267415.7:n.1129+38T=
ENST00000646753.1:c.1024+38T= ENSP00000494065.1:n.1024+38T=
ENST00000267415.11:c.1129+38T= ENSP00000267415.7:n.1129+38T=
ENST00000399423.8:c.*190T= ENSP00000382350.4:n.*190T=
ENST00000557915.1:n.336+38T=
ENST00000558566.1:c.*627T= ENSP00000453025.1:n.*627T=
ENST00000558703.1:n.18T=
ENST00000559969.5:c.1013T=
ENST00000560019.5:c.124+38T= ENSP00000453113.1:n.124+38T=
ENST00000626689.2:c.*501+38T= ENSP00000486681.1:n.*501+38T=
NM_001099274.1:c.1129+38T= NP_001092744.1:n.1129+38T=
NM_012461.2:c.*190T= NP_036593.2:n.*190T=
XM_005267528.2:c.1129+38T= XP_005267585.1:n.1129+38T=
XM_005267529.2:c.1024+38T= XP_005267586.1:n.1024+38T=
NM_001099274.2:c.1129+38T= NP_001092744.1:n.1129+38T=
NM_001363668.1:c.1024+38T= NP_001350597.1:n.1024+38T=
NM_012461.3:c.*190T= NP_036593.2:n.*190T=
XM_011536642.2:c.*635T= XP_011534944.1:n.*635T=
XM_017021216.2:c.487+38T= XP_016876705.1:n.487+38T=
XM_017021217.1:c.487+38T= XP_016876706.1:n.487+38T=
NM_001099274.3:c.1129+38T= MANE Select NP_001092744.1:n.1129+38T=
NM_001363668.2:c.1024+38T= NP_001350597.1:n.1024+38T=