Canonical Allele Identifier: CA2123849327
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240679T= , CM000676.2:g.24240679T= GRCh38
NC_000014.8:g.24709885T= , CM000676.1:g.24709885T= GRCh37
NC_000014.7:g.23779725T= NCBI36
NG_016650.1:g.6996A=
NG_054634.1:g.13263T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1104A=
ENST00000557921.3:c.693A= ENSP00000453157.3:p.Arg231=
ENST00000699682.1:n.1191A=
ENST00000699683.1:n.1241A=
ENST00000699684.1:c.*394A= ENSP00000514523.1:n.*394A=
ENST00000699685.1:n.1005A=
ENST00000699686.1:c.594A= ENSP00000514524.1:p.Arg198=
ENST00000699687.1:c.696A= ENSP00000514525.1:p.Arg232=
ENST00000699688.1:n.1001A=
ENST00000699689.1:n.1357A=
ENST00000699690.1:n.1554A=
ENST00000699691.1:n.1698A=
ENST00000699693.1:n.1218A=
ENST00000699694.1:n.1460A=
ENST00000699695.1:c.*173A= ENSP00000514526.1:n.*173A=
ENST00000699696.1:n.1104A=
ENST00000699697.1:c.801A= ENSP00000514527.1:p.Arg267=
ENST00000699698.1:n.722A=
ENST00000699699.1:n.1125A=
ENST00000699700.1:n.1248A=
ENST00000699701.1:c.*181A= ENSP00000514528.1:n.*181A=
ENST00000267415.12:c.801A= MANE Select ENSP00000267415.7:p.Arg267=
ENST00000557921.2:c.693A= ENSP00000453157.2:p.Arg231=
ENST00000646753.1:c.696A= ENSP00000494065.1:p.Arg232=
ENST00000267415.11:c.801A= ENSP00000267415.7:p.Arg267=
ENST00000399423.8:c.801A= ENSP00000382350.4:p.Arg267=
ENST00000558476.5:c.363A= ENSP00000452724.1:p.Arg121=
ENST00000558566.1:c.*173A= ENSP00000453025.1:n.*173A=
ENST00000559019.1:c.*173A= ENSP00000453675.1:n.*173A=
ENST00000559549.1:n.527A=
ENST00000559969.5:c.757A=
ENST00000626689.2:c.*173A= ENSP00000486681.1:n.*173A=
NM_001099274.1:c.801A= NP_001092744.1:p.Arg267=
NM_012461.2:c.801A= NP_036593.2:p.Arg267=
XM_005267528.2:c.801A= XP_005267585.1:p.Arg267=
XM_005267529.2:c.696A= XP_005267586.1:p.Arg232=
NM_001099274.2:c.801A= NP_001092744.1:p.Arg267=
NM_001363668.1:c.696A= NP_001350597.1:p.Arg232=
NM_012461.3:c.801A= NP_036593.2:p.Arg267=
XM_011536642.2:c.*181A= XP_011534944.1:n.*181A=
XM_017021216.2:c.159A= XP_016876705.1:p.Arg53=
XM_017021217.1:c.159A= XP_016876706.1:p.Arg53=
NM_001099274.3:c.801A= MANE Select NP_001092744.1:p.Arg267=
NM_001363668.2:c.696A= NP_001350597.1:p.Arg232=