Canonical Allele Identifier: CA2123849248
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240527A= , CM000676.2:g.24240527A= GRCh38
NC_000014.8:g.24709733A= , CM000676.1:g.24709733A= GRCh37
NC_000014.7:g.23779573A= NCBI36
NG_016650.1:g.7148T=
NG_054634.1:g.13111A=

Transcript Alleles

HGVS Amino-acid change
ENST00000557915.2:n.1256T=
ENST00000557921.3:c.845T= ENSP00000453157.3:p.Met282=
ENST00000699682.1:n.1343T=
ENST00000699683.1:n.1393T=
ENST00000699684.1:c.*546T= ENSP00000514523.1:n.*546T=
ENST00000699685.1:n.1157T=
ENST00000699686.1:c.746T= ENSP00000514524.1:p.Met249=
ENST00000699687.1:c.848T= ENSP00000514525.1:p.Met283=
ENST00000699688.1:n.1153T=
ENST00000699689.1:n.1509T=
ENST00000699690.1:n.1706T=
ENST00000699691.1:n.1850T=
ENST00000699693.1:n.1370T=
ENST00000699694.1:n.1612T=
ENST00000699695.1:c.*325T= ENSP00000514526.1:n.*325T=
ENST00000699696.1:n.1256T=
ENST00000699697.1:c.953T= ENSP00000514527.1:p.Met318=
ENST00000699698.1:n.874T=
ENST00000699699.1:n.1277T=
ENST00000699700.1:n.1400T=
ENST00000699701.1:c.*333T= ENSP00000514528.1:n.*333T=
ENST00000267415.12:c.953T= MANE Select ENSP00000267415.7:p.Met318=
ENST00000557921.2:c.845T= ENSP00000453157.2:p.Met282=
ENST00000646753.1:c.848T= ENSP00000494065.1:p.Met283=
ENST00000267415.11:c.953T= ENSP00000267415.7:p.Met318=
ENST00000399423.8:c.953T= ENSP00000382350.4:p.Met318=
ENST00000557915.1:n.72T=
ENST00000558566.1:c.*325T= ENSP00000453025.1:n.*325T=
ENST00000559019.1:c.*325T= ENSP00000453675.1:n.*325T=
ENST00000559969.5:c.758-47T=
ENST00000626689.2:c.*325T= ENSP00000486681.1:n.*325T=
NM_001099274.1:c.953T= NP_001092744.1:p.Met318=
NM_012461.2:c.953T= NP_036593.2:p.Met318=
XM_005267528.2:c.953T= XP_005267585.1:p.Met318=
XM_005267529.2:c.848T= XP_005267586.1:p.Met283=
NM_001099274.2:c.953T= NP_001092744.1:p.Met318=
NM_001363668.1:c.848T= NP_001350597.1:p.Met283=
NM_012461.3:c.953T= NP_036593.2:p.Met318=
XM_011536642.2:c.*333T= XP_011534944.1:n.*333T=
XM_017021216.2:c.311T= XP_016876705.1:p.Met104=
XM_017021217.1:c.311T= XP_016876706.1:p.Met104=
NM_001099274.3:c.953T= MANE Select NP_001092744.1:p.Met318=
NM_001363668.2:c.848T= NP_001350597.1:p.Met283=