Canonical Allele Identifier: CA2123848924
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240311T= , CM000676.2:g.24240311T= GRCh38
NC_000014.8:g.24709517T= , CM000676.1:g.24709517T= GRCh37
NC_000014.7:g.23779357T= NCBI36
NG_016650.1:g.7364A=
NG_054634.1:g.12895T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1472A=
ENST00000557921.3:c.*104A= ENSP00000453157.3:n.*104A=
ENST00000699682.1:n.1559A=
ENST00000699683.1:n.1609A=
ENST00000699684.1:c.*762A= ENSP00000514523.1:n.*762A=
ENST00000699685.1:n.1373A=
ENST00000699686.1:c.*104A= ENSP00000514524.1:n.*104A=
ENST00000699687.1:c.*104A= ENSP00000514525.1:n.*104A=
ENST00000699688.1:n.1369A=
ENST00000699689.1:n.1725A=
ENST00000699690.1:n.1922A=
ENST00000699691.1:n.2066A=
ENST00000699692.1:n.20A=
ENST00000699693.1:n.1498A=
ENST00000699694.1:n.1828A=
ENST00000699695.1:c.*453A= ENSP00000514526.1:n.*453A=
ENST00000699696.1:n.1472A=
ENST00000699697.1:c.1081A= ENSP00000514527.1:p.Met361=
ENST00000699698.1:n.1002A=
ENST00000699699.1:n.1493A=
ENST00000699700.1:n.1616A=
ENST00000699701.1:c.*549A= ENSP00000514528.1:n.*549A=
ENST00000267415.12:c.1081A= MANE Select ENSP00000267415.7:p.Met361=
ENST00000646753.1:c.976A= ENSP00000494065.1:p.Met326=
ENST00000267415.11:c.1081A= ENSP00000267415.7:p.Met361=
ENST00000399423.8:c.*104A= ENSP00000382350.4:n.*104A=
ENST00000557915.1:n.288A=
ENST00000558566.1:c.*541A= ENSP00000453025.1:n.*541A=
ENST00000559969.5:c.927A=
ENST00000560019.5:c.76A= ENSP00000453113.1:p.Met26=
ENST00000626689.2:c.*453A= ENSP00000486681.1:n.*453A=
NM_001099274.1:c.1081A= NP_001092744.1:p.Met361=
NM_012461.2:c.*104A= NP_036593.2:n.*104A=
XM_005267528.2:c.1081A= XP_005267585.1:p.Met361=
XM_005267529.2:c.976A= XP_005267586.1:p.Met326=
NM_001099274.2:c.1081A= NP_001092744.1:p.Met361=
NM_001363668.1:c.976A= NP_001350597.1:p.Met326=
NM_012461.3:c.*104A= NP_036593.2:n.*104A=
XM_011536642.2:c.*549A= XP_011534944.1:n.*549A=
XM_017021216.2:c.439A= XP_016876705.1:p.Met147=
XM_017021217.1:c.439A= XP_016876706.1:p.Met147=
NM_001099274.3:c.1081A= MANE Select NP_001092744.1:p.Met361=
NM_001363668.2:c.976A= NP_001350597.1:p.Met326=