Canonical Allele Identifier: CA2123848835
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240292G= , CM000676.2:g.24240292G= GRCh38
NC_000014.8:g.24709498G= , CM000676.1:g.24709498G= GRCh37
NC_000014.7:g.23779338G= NCBI36
NG_016650.1:g.7383C=
NG_054634.1:g.12876G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1491C=
ENST00000557921.3:c.*123C= ENSP00000453157.3:n.*123C=
ENST00000699682.1:n.1578C=
ENST00000699683.1:n.1628C=
ENST00000699684.1:c.*781C= ENSP00000514523.1:n.*781C=
ENST00000699685.1:n.1392C=
ENST00000699686.1:c.*123C= ENSP00000514524.1:n.*123C=
ENST00000699687.1:c.*123C= ENSP00000514525.1:n.*123C=
ENST00000699688.1:n.1388C=
ENST00000699689.1:n.1744C=
ENST00000699690.1:n.1941C=
ENST00000699691.1:n.2085C=
ENST00000699692.1:n.39C=
ENST00000699693.1:n.1517C=
ENST00000699694.1:n.1847C=
ENST00000699695.1:c.*472C= ENSP00000514526.1:n.*472C=
ENST00000699696.1:n.1491C=
ENST00000699697.1:c.1100C= ENSP00000514527.1:p.Ser367=
ENST00000699698.1:n.1021C=
ENST00000699699.1:n.1512C=
ENST00000699700.1:n.1635C=
ENST00000699701.1:c.*568C= ENSP00000514528.1:n.*568C=
ENST00000267415.12:c.1100C= MANE Select ENSP00000267415.7:p.Ser367=
ENST00000646753.1:c.995C= ENSP00000494065.1:p.Ser332=
ENST00000267415.11:c.1100C= ENSP00000267415.7:p.Ser367=
ENST00000399423.8:c.*123C= ENSP00000382350.4:n.*123C=
ENST00000557915.1:n.307C=
ENST00000558566.1:c.*560C= ENSP00000453025.1:n.*560C=
ENST00000559969.5:c.946C=
ENST00000560019.5:c.95C= ENSP00000453113.1:p.Ser32=
ENST00000626689.2:c.*472C= ENSP00000486681.1:n.*472C=
NM_001099274.1:c.1100C= NP_001092744.1:p.Ser367=
NM_012461.2:c.*123C= NP_036593.2:n.*123C=
XM_005267528.2:c.1100C= XP_005267585.1:p.Ser367=
XM_005267529.2:c.995C= XP_005267586.1:p.Ser332=
NM_001099274.2:c.1100C= NP_001092744.1:p.Ser367=
NM_001363668.1:c.995C= NP_001350597.1:p.Ser332=
NM_012461.3:c.*123C= NP_036593.2:n.*123C=
XM_011536642.2:c.*568C= XP_011534944.1:n.*568C=
XM_017021216.2:c.458C= XP_016876705.1:p.Ser153=
XM_017021217.1:c.458C= XP_016876706.1:p.Ser153=
NM_001099274.3:c.1100C= MANE Select NP_001092744.1:p.Ser367=
NM_001363668.2:c.995C= NP_001350597.1:p.Ser332=