Canonical Allele Identifier: CA2123848991
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240332T= , CM000676.2:g.24240332T= GRCh38
NC_000014.8:g.24709538T= , CM000676.1:g.24709538T= GRCh37
NC_000014.7:g.23779378T= NCBI36
NG_016650.1:g.7343A=
NG_054634.1:g.12916T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1451A=
ENST00000557921.3:c.*83A= ENSP00000453157.3:n.*83A=
ENST00000699682.1:n.1538A=
ENST00000699683.1:n.1588A=
ENST00000699684.1:c.*741A= ENSP00000514523.1:n.*741A=
ENST00000699685.1:n.1352A=
ENST00000699686.1:c.*83A= ENSP00000514524.1:n.*83A=
ENST00000699687.1:c.*83A= ENSP00000514525.1:n.*83A=
ENST00000699688.1:n.1348A=
ENST00000699689.1:n.1704A=
ENST00000699690.1:n.1901A=
ENST00000699691.1:n.2045A=
ENST00000699693.1:n.1479-2A=
ENST00000699694.1:n.1807A=
ENST00000699695.1:c.*434-2A= ENSP00000514526.1:n.*434-2A=
ENST00000699696.1:n.1451A=
ENST00000699697.1:c.1062-2A= ENSP00000514527.1:n.1062-2A=
ENST00000699698.1:n.983-2A=
ENST00000699699.1:n.1472A=
ENST00000699700.1:n.1595A=
ENST00000699701.1:c.*528A= ENSP00000514528.1:n.*528A=
ENST00000267415.12:c.1062-2A= MANE Select ENSP00000267415.7:n.1062-2A=
ENST00000646753.1:c.957-2A= ENSP00000494065.1:n.957-2A=
ENST00000267415.11:c.1062-2A= ENSP00000267415.7:n.1062-2A=
ENST00000399423.8:c.*83A= ENSP00000382350.4:n.*83A=
ENST00000557915.1:n.267A=
ENST00000558566.1:c.*520A= ENSP00000453025.1:n.*520A=
ENST00000559969.5:c.906A=
ENST00000560019.5:c.57-2A= ENSP00000453113.1:n.57-2A=
ENST00000626689.2:c.*434-2A= ENSP00000486681.1:n.*434-2A=
NM_001099274.1:c.1062-2A= NP_001092744.1:n.1062-2A=
NM_012461.2:c.*83A= NP_036593.2:n.*83A=
XM_005267528.2:c.1062-2A= XP_005267585.1:n.1062-2A=
XM_005267529.2:c.957-2A= XP_005267586.1:n.957-2A=
NM_001099274.2:c.1062-2A= NP_001092744.1:n.1062-2A=
NM_001363668.1:c.957-2A= NP_001350597.1:n.957-2A=
NM_012461.3:c.*83A= NP_036593.2:n.*83A=
XM_011536642.2:c.*528A= XP_011534944.1:n.*528A=
XM_017021216.2:c.420-2A= XP_016876705.1:n.420-2A=
XM_017021217.1:c.420-2A= XP_016876706.1:n.420-2A=
NM_001099274.3:c.1062-2A= MANE Select NP_001092744.1:n.1062-2A=
NM_001363668.2:c.957-2A= NP_001350597.1:n.957-2A=