Canonical Allele Identifier: CA2123849340
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240704T= , CM000676.2:g.24240704T= GRCh38
NC_000014.8:g.24709910T= , CM000676.1:g.24709910T= GRCh37
NC_000014.7:g.23779750T= NCBI36
NG_016650.1:g.6971A=
NG_054634.1:g.13288T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1079A=
ENST00000557921.3:c.668A= ENSP00000453157.3:p.Asn223=
ENST00000699682.1:n.1166A=
ENST00000699683.1:n.1216A=
ENST00000699684.1:c.*369A= ENSP00000514523.1:n.*369A=
ENST00000699685.1:n.980A=
ENST00000699686.1:c.569A= ENSP00000514524.1:p.Asn190=
ENST00000699687.1:c.671A= ENSP00000514525.1:p.Asn224=
ENST00000699688.1:n.976A=
ENST00000699689.1:n.1332A=
ENST00000699690.1:n.1529A=
ENST00000699691.1:n.1673A=
ENST00000699693.1:n.1193A=
ENST00000699694.1:n.1435A=
ENST00000699695.1:c.*148A= ENSP00000514526.1:n.*148A=
ENST00000699696.1:n.1079A=
ENST00000699697.1:c.776A= ENSP00000514527.1:p.Asn259=
ENST00000699698.1:n.697A=
ENST00000699699.1:n.1100A=
ENST00000699700.1:n.1223A=
ENST00000699701.1:c.*156A= ENSP00000514528.1:n.*156A=
ENST00000267415.12:c.776A= MANE Select ENSP00000267415.7:p.Asn259=
ENST00000557921.2:c.668A= ENSP00000453157.2:p.Asn223=
ENST00000646753.1:c.671A= ENSP00000494065.1:p.Asn224=
ENST00000267415.11:c.776A= ENSP00000267415.7:p.Asn259=
ENST00000399423.8:c.776A= ENSP00000382350.4:p.Asn259=
ENST00000558476.5:c.338A= ENSP00000452724.1:p.Asn113=
ENST00000558566.1:c.*148A= ENSP00000453025.1:n.*148A=
ENST00000559019.1:c.*148A= ENSP00000453675.1:n.*148A=
ENST00000559549.1:n.502A=
ENST00000559969.5:c.732A=
ENST00000626689.2:c.*148A= ENSP00000486681.1:n.*148A=
NM_001099274.1:c.776A= NP_001092744.1:p.Asn259=
NM_012461.2:c.776A= NP_036593.2:p.Asn259=
XM_005267528.2:c.776A= XP_005267585.1:p.Asn259=
XM_005267529.2:c.671A= XP_005267586.1:p.Asn224=
NM_001099274.2:c.776A= NP_001092744.1:p.Asn259=
NM_001363668.1:c.671A= NP_001350597.1:p.Asn224=
NM_012461.3:c.776A= NP_036593.2:p.Asn259=
XM_011536642.2:c.*156A= XP_011534944.1:n.*156A=
XM_017021216.2:c.134A= XP_016876705.1:p.Asn45=
XM_017021217.1:c.134A= XP_016876706.1:p.Asn45=
NM_001099274.3:c.776A= MANE Select NP_001092744.1:p.Asn259=
NM_001363668.2:c.671A= NP_001350597.1:p.Asn224=