Canonical Allele Identifier: CA2123848756
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240247G= , CM000676.2:g.24240247G= GRCh38
NC_000014.8:g.24709453G= , CM000676.1:g.24709453G= GRCh37
NC_000014.7:g.23779293G= NCBI36
NG_016650.1:g.7428C=
NG_054634.1:g.12831G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1520+16C=
ENST00000557921.3:c.*168C= ENSP00000453157.3:n.*168C=
ENST00000699682.1:n.1623C=
ENST00000699683.1:n.1673C=
ENST00000699684.1:c.*826C= ENSP00000514523.1:n.*826C=
ENST00000699685.1:n.1437C=
ENST00000699686.1:c.*168C= ENSP00000514524.1:n.*168C=
ENST00000699687.1:c.*168C= ENSP00000514525.1:n.*168C=
ENST00000699688.1:n.1433C=
ENST00000699689.1:n.1789C=
ENST00000699690.1:n.1986C=
ENST00000699691.1:n.2130C=
ENST00000699692.1:n.68+16C=
ENST00000699693.1:n.1546+16C=
ENST00000699694.1:n.1892C=
ENST00000699695.1:c.*501+16C= ENSP00000514526.1:n.*501+16C=
ENST00000699696.1:n.1520+16C=
ENST00000699697.1:c.*8C= ENSP00000514527.1:n.*8C=
ENST00000699698.1:n.1066C=
ENST00000699699.1:n.1557C=
ENST00000699700.1:n.1680C=
ENST00000699701.1:c.*613C= ENSP00000514528.1:n.*613C=
ENST00000267415.12:c.1129+16C= MANE Select ENSP00000267415.7:n.1129+16C=
ENST00000646753.1:c.1024+16C= ENSP00000494065.1:n.1024+16C=
ENST00000267415.11:c.1129+16C= ENSP00000267415.7:n.1129+16C=
ENST00000399423.8:c.*168C= ENSP00000382350.4:n.*168C=
ENST00000557915.1:n.336+16C=
ENST00000558566.1:c.*605C= ENSP00000453025.1:n.*605C=
ENST00000559969.5:c.991C=
ENST00000560019.5:c.124+16C= ENSP00000453113.1:n.124+16C=
ENST00000626689.2:c.*501+16C= ENSP00000486681.1:n.*501+16C=
NM_001099274.1:c.1129+16C= NP_001092744.1:n.1129+16C=
NM_012461.2:c.*168C= NP_036593.2:n.*168C=
XM_005267528.2:c.1129+16C= XP_005267585.1:n.1129+16C=
XM_005267529.2:c.1024+16C= XP_005267586.1:n.1024+16C=
NM_001099274.2:c.1129+16C= NP_001092744.1:n.1129+16C=
NM_001363668.1:c.1024+16C= NP_001350597.1:n.1024+16C=
NM_012461.3:c.*168C= NP_036593.2:n.*168C=
XM_011536642.2:c.*613C= XP_011534944.1:n.*613C=
XM_017021216.2:c.487+16C= XP_016876705.1:n.487+16C=
XM_017021217.1:c.487+16C= XP_016876706.1:n.487+16C=
NM_001099274.3:c.1129+16C= MANE Select NP_001092744.1:n.1129+16C=
NM_001363668.2:c.1024+16C= NP_001350597.1:n.1024+16C=