Canonical Allele Identifier: CA2123849278
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240575T= , CM000676.2:g.24240575T= GRCh38
NC_000014.8:g.24709781T= , CM000676.1:g.24709781T= GRCh37
NC_000014.7:g.23779621T= NCBI36
NG_016650.1:g.7100A=
NG_054634.1:g.13159T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1208A=
ENST00000557921.3:c.797A= ENSP00000453157.3:p.Lys266=
ENST00000699682.1:n.1295A=
ENST00000699683.1:n.1345A=
ENST00000699684.1:c.*498A= ENSP00000514523.1:n.*498A=
ENST00000699685.1:n.1109A=
ENST00000699686.1:c.698A= ENSP00000514524.1:p.Lys233=
ENST00000699687.1:c.800A= ENSP00000514525.1:p.Lys267=
ENST00000699688.1:n.1105A=
ENST00000699689.1:n.1461A=
ENST00000699690.1:n.1658A=
ENST00000699691.1:n.1802A=
ENST00000699693.1:n.1322A=
ENST00000699694.1:n.1564A=
ENST00000699695.1:c.*277A= ENSP00000514526.1:n.*277A=
ENST00000699696.1:n.1208A=
ENST00000699697.1:c.905A= ENSP00000514527.1:p.Lys302=
ENST00000699698.1:n.826A=
ENST00000699699.1:n.1229A=
ENST00000699700.1:n.1352A=
ENST00000699701.1:c.*285A= ENSP00000514528.1:n.*285A=
ENST00000267415.12:c.905A= MANE Select ENSP00000267415.7:p.Lys302=
ENST00000557921.2:c.797A= ENSP00000453157.2:p.Lys266=
ENST00000646753.1:c.800A= ENSP00000494065.1:p.Lys267=
ENST00000267415.11:c.905A= ENSP00000267415.7:p.Lys302=
ENST00000399423.8:c.905A= ENSP00000382350.4:p.Lys302=
ENST00000557915.1:n.24A=
ENST00000558566.1:c.*277A= ENSP00000453025.1:n.*277A=
ENST00000559019.1:c.*277A= ENSP00000453675.1:n.*277A=
ENST00000559969.5:c.758-95A=
ENST00000626689.2:c.*277A= ENSP00000486681.1:n.*277A=
NM_001099274.1:c.905A= NP_001092744.1:p.Lys302=
NM_012461.2:c.905A= NP_036593.2:p.Lys302=
XM_005267528.2:c.905A= XP_005267585.1:p.Lys302=
XM_005267529.2:c.800A= XP_005267586.1:p.Lys267=
NM_001099274.2:c.905A= NP_001092744.1:p.Lys302=
NM_001363668.1:c.800A= NP_001350597.1:p.Lys267=
NM_012461.3:c.905A= NP_036593.2:p.Lys302=
XM_011536642.2:c.*285A= XP_011534944.1:n.*285A=
XM_017021216.2:c.263A= XP_016876705.1:p.Lys88=
XM_017021217.1:c.263A= XP_016876706.1:p.Lys88=
NM_001099274.3:c.905A= MANE Select NP_001092744.1:p.Lys302=
NM_001363668.2:c.800A= NP_001350597.1:p.Lys267=