Canonical Allele Identifier: CA2123849050
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240372C= , CM000676.2:g.24240372C= GRCh38
NC_000014.8:g.24709578C= , CM000676.1:g.24709578C= GRCh37
NC_000014.7:g.23779418C= NCBI36
NG_016650.1:g.7303G=
NG_054634.1:g.12956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1411G=
ENST00000557921.3:c.*43G= ENSP00000453157.3:n.*43G=
ENST00000699682.1:n.1498G=
ENST00000699683.1:n.1548G=
ENST00000699684.1:c.*701G= ENSP00000514523.1:n.*701G=
ENST00000699685.1:n.1312G=
ENST00000699686.1:c.*43G= ENSP00000514524.1:n.*43G=
ENST00000699687.1:c.*43G= ENSP00000514525.1:n.*43G=
ENST00000699688.1:n.1308G=
ENST00000699689.1:n.1664G=
ENST00000699690.1:n.1861G=
ENST00000699691.1:n.2005G=
ENST00000699693.1:n.1479-42G=
ENST00000699694.1:n.1767G=
ENST00000699695.1:c.*434-42G= ENSP00000514526.1:n.*434-42G=
ENST00000699696.1:n.1411G=
ENST00000699697.1:c.1062-42G= ENSP00000514527.1:n.1062-42G=
ENST00000699698.1:n.983-42G=
ENST00000699699.1:n.1432G=
ENST00000699700.1:n.1555G=
ENST00000699701.1:c.*488G= ENSP00000514528.1:n.*488G=
ENST00000267415.12:c.1062-42G= MANE Select ENSP00000267415.7:n.1062-42G=
ENST00000646753.1:c.957-42G= ENSP00000494065.1:n.957-42G=
ENST00000267415.11:c.1062-42G= ENSP00000267415.7:n.1062-42G=
ENST00000399423.8:c.*43G= ENSP00000382350.4:n.*43G=
ENST00000557915.1:n.227G=
ENST00000558566.1:c.*480G= ENSP00000453025.1:n.*480G=
ENST00000559969.5:c.866G=
ENST00000560019.5:c.57-42G= ENSP00000453113.1:n.57-42G=
ENST00000626689.2:c.*434-42G= ENSP00000486681.1:n.*434-42G=
NM_001099274.1:c.1062-42G= NP_001092744.1:n.1062-42G=
NM_012461.2:c.*43G= NP_036593.2:n.*43G=
XM_005267528.2:c.1062-42G= XP_005267585.1:n.1062-42G=
XM_005267529.2:c.957-42G= XP_005267586.1:n.957-42G=
NM_001099274.2:c.1062-42G= NP_001092744.1:n.1062-42G=
NM_001363668.1:c.957-42G= NP_001350597.1:n.957-42G=
NM_012461.3:c.*43G= NP_036593.2:n.*43G=
XM_011536642.2:c.*488G= XP_011534944.1:n.*488G=
XM_017021216.2:c.420-42G= XP_016876705.1:n.420-42G=
XM_017021217.1:c.420-42G= XP_016876706.1:n.420-42G=
NM_001099274.3:c.1062-42G= MANE Select NP_001092744.1:n.1062-42G=
NM_001363668.2:c.957-42G= NP_001350597.1:n.957-42G=