Canonical Allele Identifier: CA2123849279
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240578G= , CM000676.2:g.24240578G= GRCh38
NC_000014.8:g.24709784G= , CM000676.1:g.24709784G= GRCh37
NC_000014.7:g.23779624G= NCBI36
NG_016650.1:g.7097C=
NG_054634.1:g.13162G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1205C=
ENST00000557921.3:c.794C= ENSP00000453157.3:p.Ser265=
ENST00000699682.1:n.1292C=
ENST00000699683.1:n.1342C=
ENST00000699684.1:c.*495C= ENSP00000514523.1:n.*495C=
ENST00000699685.1:n.1106C=
ENST00000699686.1:c.695C= ENSP00000514524.1:p.Ser232=
ENST00000699687.1:c.797C= ENSP00000514525.1:p.Ser266=
ENST00000699688.1:n.1102C=
ENST00000699689.1:n.1458C=
ENST00000699690.1:n.1655C=
ENST00000699691.1:n.1799C=
ENST00000699693.1:n.1319C=
ENST00000699694.1:n.1561C=
ENST00000699695.1:c.*274C= ENSP00000514526.1:n.*274C=
ENST00000699696.1:n.1205C=
ENST00000699697.1:c.902C= ENSP00000514527.1:p.Ser301=
ENST00000699698.1:n.823C=
ENST00000699699.1:n.1226C=
ENST00000699700.1:n.1349C=
ENST00000699701.1:c.*282C= ENSP00000514528.1:n.*282C=
ENST00000267415.12:c.902C= MANE Select ENSP00000267415.7:p.Ser301=
ENST00000557921.2:c.794C= ENSP00000453157.2:p.Ser265=
ENST00000646753.1:c.797C= ENSP00000494065.1:p.Ser266=
ENST00000267415.11:c.902C= ENSP00000267415.7:p.Ser301=
ENST00000399423.8:c.902C= ENSP00000382350.4:p.Ser301=
ENST00000557915.1:n.21C=
ENST00000558566.1:c.*274C= ENSP00000453025.1:n.*274C=
ENST00000559019.1:c.*274C= ENSP00000453675.1:n.*274C=
ENST00000559969.5:c.758-98C=
ENST00000626689.2:c.*274C= ENSP00000486681.1:n.*274C=
NM_001099274.1:c.902C= NP_001092744.1:p.Ser301=
NM_012461.2:c.902C= NP_036593.2:p.Ser301=
XM_005267528.2:c.902C= XP_005267585.1:p.Ser301=
XM_005267529.2:c.797C= XP_005267586.1:p.Ser266=
NM_001099274.2:c.902C= NP_001092744.1:p.Ser301=
NM_001363668.1:c.797C= NP_001350597.1:p.Ser266=
NM_012461.3:c.902C= NP_036593.2:p.Ser301=
XM_011536642.2:c.*282C= XP_011534944.1:n.*282C=
XM_017021216.2:c.260C= XP_016876705.1:p.Ser87=
XM_017021217.1:c.260C= XP_016876706.1:p.Ser87=
NM_001099274.3:c.902C= MANE Select NP_001092744.1:p.Ser301=
NM_001363668.2:c.797C= NP_001350597.1:p.Ser266=