Canonical Allele Identifier: CA2123849325
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240678C= , CM000676.2:g.24240678C= GRCh38
NC_000014.8:g.24709884C= , CM000676.1:g.24709884C= GRCh37
NC_000014.7:g.23779724C= NCBI36
NG_016650.1:g.6997G=
NG_054634.1:g.13262C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1105G=
ENST00000557921.3:c.694G= ENSP00000453157.3:p.Val232=
ENST00000699682.1:n.1192G=
ENST00000699683.1:n.1242G=
ENST00000699684.1:c.*395G= ENSP00000514523.1:n.*395G=
ENST00000699685.1:n.1006G=
ENST00000699686.1:c.595G= ENSP00000514524.1:p.Val199=
ENST00000699687.1:c.697G= ENSP00000514525.1:p.Val233=
ENST00000699688.1:n.1002G=
ENST00000699689.1:n.1358G=
ENST00000699690.1:n.1555G=
ENST00000699691.1:n.1699G=
ENST00000699693.1:n.1219G=
ENST00000699694.1:n.1461G=
ENST00000699695.1:c.*174G= ENSP00000514526.1:n.*174G=
ENST00000699696.1:n.1105G=
ENST00000699697.1:c.802G= ENSP00000514527.1:p.Val268=
ENST00000699698.1:n.723G=
ENST00000699699.1:n.1126G=
ENST00000699700.1:n.1249G=
ENST00000699701.1:c.*182G= ENSP00000514528.1:n.*182G=
ENST00000267415.12:c.802G= MANE Select ENSP00000267415.7:p.Val268=
ENST00000557921.2:c.694G= ENSP00000453157.2:p.Val232=
ENST00000646753.1:c.697G= ENSP00000494065.1:p.Val233=
ENST00000267415.11:c.802G= ENSP00000267415.7:p.Val268=
ENST00000399423.8:c.802G= ENSP00000382350.4:p.Val268=
ENST00000558476.5:c.364G= ENSP00000452724.1:p.Val122=
ENST00000558566.1:c.*174G= ENSP00000453025.1:n.*174G=
ENST00000559019.1:c.*174G= ENSP00000453675.1:n.*174G=
ENST00000559549.1:n.528G=
ENST00000559969.5:c.757+1G=
ENST00000626689.2:c.*174G= ENSP00000486681.1:n.*174G=
NM_001099274.1:c.802G= NP_001092744.1:p.Val268=
NM_012461.2:c.802G= NP_036593.2:p.Val268=
XM_005267528.2:c.802G= XP_005267585.1:p.Val268=
XM_005267529.2:c.697G= XP_005267586.1:p.Val233=
NM_001099274.2:c.802G= NP_001092744.1:p.Val268=
NM_001363668.1:c.697G= NP_001350597.1:p.Val233=
NM_012461.3:c.802G= NP_036593.2:p.Val268=
XM_011536642.2:c.*182G= XP_011534944.1:n.*182G=
XM_017021216.2:c.160G= XP_016876705.1:p.Val54=
XM_017021217.1:c.160G= XP_016876706.1:p.Val54=
NM_001099274.3:c.802G= MANE Select NP_001092744.1:p.Val268=
NM_001363668.2:c.697G= NP_001350597.1:p.Val233=