Canonical Allele Identifier: CA389224223
Gene: TINF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240521G>T , CM000676.2:g.24240521G>T GRCh38
NC_000014.8:g.24709727G>T , CM000676.1:g.24709727G>T GRCh37
NC_000014.7:g.23779567G>T NCBI36
NG_016650.1:g.7154C>A
NG_054634.1:g.13105G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000557915.2:n.1262C>A
ENST00000557921.3:c.851C>A ENSP00000453157.3:p.Thr284Lys
ENST00000699682.1:n.1349C>A
ENST00000699683.1:n.1399C>A
ENST00000699684.1:c.*552C>A ENSP00000514523.1:n.*552C>A
ENST00000699685.1:n.1163C>A
ENST00000699686.1:c.752C>A ENSP00000514524.1:p.Thr251Lys
ENST00000699687.1:c.854C>A ENSP00000514525.1:p.Thr285Lys
ENST00000699688.1:n.1159C>A
ENST00000699689.1:n.1515C>A
ENST00000699690.1:n.1712C>A
ENST00000699691.1:n.1856C>A
ENST00000699693.1:n.1376C>A
ENST00000699694.1:n.1618C>A
ENST00000699695.1:c.*331C>A ENSP00000514526.1:n.*331C>A
ENST00000699696.1:n.1262C>A
ENST00000699697.1:c.959C>A ENSP00000514527.1:p.Thr320Lys
ENST00000699698.1:n.880C>A
ENST00000699699.1:n.1283C>A
ENST00000699700.1:n.1406C>A
ENST00000699701.1:c.*339C>A ENSP00000514528.1:n.*339C>A
ENST00000267415.12:c.959C>A MANE Select ENSP00000267415.7:p.Thr320Lys
ENST00000557921.2:c.851C>A ENSP00000453157.2:p.Thr284Lys
ENST00000646753.1:c.854C>A ENSP00000494065.1:p.Thr285Lys
ENST00000267415.11:c.959C>A ENSP00000267415.7:p.Thr320Lys
ENST00000399423.8:c.959C>A ENSP00000382350.4:p.Thr320Lys
ENST00000557915.1:n.78C>A
ENST00000558566.1:c.*331C>A ENSP00000453025.1:n.*331C>A
ENST00000559019.1:c.*331C>A ENSP00000453675.1:n.*331C>A
ENST00000559969.5:c.758-41C>A
ENST00000626689.2:c.*331C>A ENSP00000486681.1:n.*331C>A
NM_001099274.1:c.959C>A NP_001092744.1:p.Thr320Lys
NM_012461.2:c.959C>A NP_036593.2:p.Thr320Lys
XM_005267528.2:c.959C>A XP_005267585.1:p.Thr320Lys
XM_005267529.2:c.854C>A XP_005267586.1:p.Thr285Lys
NM_001099274.2:c.959C>A NP_001092744.1:p.Thr320Lys
NM_001363668.1:c.854C>A NP_001350597.1:p.Thr285Lys
NM_012461.3:c.959C>A NP_036593.2:p.Thr320Lys
XM_011536642.2:c.*339C>A XP_011534944.1:n.*339C>A
XM_017021216.2:c.317C>A XP_016876705.1:p.Thr106Lys
XM_017021217.1:c.317C>A XP_016876706.1:p.Thr106Lys
NM_001099274.3:c.959C>A MANE Select NP_001092744.1:p.Thr320Lys
NM_001363668.2:c.854C>A NP_001350597.1:p.Thr285Lys