Canonical Allele Identifier: CA2123849324
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240675G= , CM000676.2:g.24240675G= GRCh38
NC_000014.8:g.24709881G= , CM000676.1:g.24709881G= GRCh37
NC_000014.7:g.23779721G= NCBI36
NG_016650.1:g.7000C=
NG_054634.1:g.13259G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1108C=
ENST00000557921.3:c.697C= ENSP00000453157.3:p.Gln233=
ENST00000699682.1:n.1195C=
ENST00000699683.1:n.1245C=
ENST00000699684.1:c.*398C= ENSP00000514523.1:n.*398C=
ENST00000699685.1:n.1009C=
ENST00000699686.1:c.598C= ENSP00000514524.1:p.Gln200=
ENST00000699687.1:c.700C= ENSP00000514525.1:p.Gln234=
ENST00000699688.1:n.1005C=
ENST00000699689.1:n.1361C=
ENST00000699690.1:n.1558C=
ENST00000699691.1:n.1702C=
ENST00000699693.1:n.1222C=
ENST00000699694.1:n.1464C=
ENST00000699695.1:c.*177C= ENSP00000514526.1:n.*177C=
ENST00000699696.1:n.1108C=
ENST00000699697.1:c.805C= ENSP00000514527.1:p.Gln269=
ENST00000699698.1:n.726C=
ENST00000699699.1:n.1129C=
ENST00000699700.1:n.1252C=
ENST00000699701.1:c.*185C= ENSP00000514528.1:n.*185C=
ENST00000267415.12:c.805C= MANE Select ENSP00000267415.7:p.Gln269=
ENST00000557921.2:c.697C= ENSP00000453157.2:p.Gln233=
ENST00000646753.1:c.700C= ENSP00000494065.1:p.Gln234=
ENST00000267415.11:c.805C= ENSP00000267415.7:p.Gln269=
ENST00000399423.8:c.805C= ENSP00000382350.4:p.Gln269=
ENST00000558476.5:c.367C= ENSP00000452724.1:p.Gln123=
ENST00000558566.1:c.*177C= ENSP00000453025.1:n.*177C=
ENST00000559019.1:c.*177C= ENSP00000453675.1:n.*177C=
ENST00000559549.1:n.531C=
ENST00000559969.5:c.757+4C=
ENST00000626689.2:c.*177C= ENSP00000486681.1:n.*177C=
NM_001099274.1:c.805C= NP_001092744.1:p.Gln269=
NM_012461.2:c.805C= NP_036593.2:p.Gln269=
XM_005267528.2:c.805C= XP_005267585.1:p.Gln269=
XM_005267529.2:c.700C= XP_005267586.1:p.Gln234=
NM_001099274.2:c.805C= NP_001092744.1:p.Gln269=
NM_001363668.1:c.700C= NP_001350597.1:p.Gln234=
NM_012461.3:c.805C= NP_036593.2:p.Gln269=
XM_011536642.2:c.*185C= XP_011534944.1:n.*185C=
XM_017021216.2:c.163C= XP_016876705.1:p.Gln55=
XM_017021217.1:c.163C= XP_016876706.1:p.Gln55=
NM_001099274.3:c.805C= MANE Select NP_001092744.1:p.Gln269=
NM_001363668.2:c.700C= NP_001350597.1:p.Gln234=