Canonical Allele Identifier: CA2123849231
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240504C= , CM000676.2:g.24240504C= GRCh38
NC_000014.8:g.24709710C= , CM000676.1:g.24709710C= GRCh37
NC_000014.7:g.23779550C= NCBI36
NG_016650.1:g.7171G=
NG_054634.1:g.13088C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1279G=
ENST00000557921.3:c.868G= ENSP00000453157.3:p.Gly290=
ENST00000699682.1:n.1366G=
ENST00000699683.1:n.1416G=
ENST00000699684.1:c.*569G= ENSP00000514523.1:n.*569G=
ENST00000699685.1:n.1180G=
ENST00000699686.1:c.769G= ENSP00000514524.1:p.Gly257=
ENST00000699687.1:c.871G= ENSP00000514525.1:p.Gly291=
ENST00000699688.1:n.1176G=
ENST00000699689.1:n.1532G=
ENST00000699690.1:n.1729G=
ENST00000699691.1:n.1873G=
ENST00000699693.1:n.1393G=
ENST00000699694.1:n.1635G=
ENST00000699695.1:c.*348G= ENSP00000514526.1:n.*348G=
ENST00000699696.1:n.1279G=
ENST00000699697.1:c.976G= ENSP00000514527.1:p.Gly326=
ENST00000699698.1:n.897G=
ENST00000699699.1:n.1300G=
ENST00000699700.1:n.1423G=
ENST00000699701.1:c.*356G= ENSP00000514528.1:n.*356G=
ENST00000267415.12:c.976G= MANE Select ENSP00000267415.7:p.Gly326=
ENST00000557921.2:c.868G= ENSP00000453157.2:p.Gly290=
ENST00000646753.1:c.871G= ENSP00000494065.1:p.Gly291=
ENST00000267415.11:c.976G= ENSP00000267415.7:p.Gly326=
ENST00000399423.8:c.976G= ENSP00000382350.4:p.Gly326=
ENST00000557915.1:n.95G=
ENST00000558566.1:c.*348G= ENSP00000453025.1:n.*348G=
ENST00000559019.1:c.*348G= ENSP00000453675.1:n.*348G=
ENST00000559969.5:c.758-24G=
ENST00000626689.2:c.*348G= ENSP00000486681.1:n.*348G=
NM_001099274.1:c.976G= NP_001092744.1:p.Gly326=
NM_012461.2:c.976G= NP_036593.2:p.Gly326=
XM_005267528.2:c.976G= XP_005267585.1:p.Gly326=
XM_005267529.2:c.871G= XP_005267586.1:p.Gly291=
NM_001099274.2:c.976G= NP_001092744.1:p.Gly326=
NM_001363668.1:c.871G= NP_001350597.1:p.Gly291=
NM_012461.3:c.976G= NP_036593.2:p.Gly326=
XM_011536642.2:c.*356G= XP_011534944.1:n.*356G=
XM_017021216.2:c.334G= XP_016876705.1:p.Gly112=
XM_017021217.1:c.334G= XP_016876706.1:p.Gly112=
NM_001099274.3:c.976G= MANE Select NP_001092744.1:p.Gly326=
NM_001363668.2:c.871G= NP_001350597.1:p.Gly291=