Canonical Allele Identifier: CA2123848745

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240234_24240237delinsTTGA , CM000676.2:g.24240234_24240237delinsTTGA	GRCh38
NC_000014.8:g.24709440_24709443delinsTTGA , CM000676.1:g.24709440_24709443delinsTTGA	GRCh37
NC_000014.7:g.23779280_23779283delinsTTGA	NCBI36
NG_016650.1:g.7438_7441delinsTCAA
NG_054634.1:g.12818_12821delinsTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1520+26_1520+29delinsTCAA
ENST00000557921.3:c.*178_*181delinsTCAA	ENSP00000453157.3:n.*178_*181delinsTCAA
ENST00000699682.1:n.1633_1636delinsTCAA
ENST00000699683.1:n.1683_1686delinsTCAA
ENST00000699684.1:c.*836_*839delinsTCAA	ENSP00000514523.1:n.*836_*839delinsTCAA
ENST00000699685.1:n.1447_1450delinsTCAA
ENST00000699686.1:c.*178_*181delinsTCAA	ENSP00000514524.1:n.*178_*181delinsTCAA
ENST00000699687.1:c.*178_*181delinsTCAA	ENSP00000514525.1:n.*178_*181delinsTCAA
ENST00000699688.1:n.1443_1446delinsTCAA
ENST00000699689.1:n.1799_1802delinsTCAA
ENST00000699690.1:n.1996_1999delinsTCAA
ENST00000699691.1:n.2140_2143delinsTCAA
ENST00000699692.1:n.68+26_68+29delinsTCAA
ENST00000699693.1:n.1546+26_1546+29delinsTCAA
ENST00000699694.1:n.1902_1905delinsTCAA
ENST00000699695.1:c.*501+26_*501+29delinsTCAA	ENSP00000514526.1:n.*501+26_*501+29delinsTCAA
ENST00000699696.1:n.1520+26_1520+29delinsTCAA
ENST00000699697.1:c.*18_*21delinsTCAA	ENSP00000514527.1:n.*18_*21delinsTCAA
ENST00000699698.1:n.1076_1079delinsTCAA
ENST00000699699.1:n.1567_1570delinsTCAA
ENST00000699700.1:n.1690_1693delinsTCAA
ENST00000699701.1:c.*623_*626delinsTCAA	ENSP00000514528.1:n.*623_*626delinsTCAA
ENST00000267415.12:c.1129+26_1129+29delinsTCAA MANE Select	ENSP00000267415.7:n.1129+26_1129+29delinsTCAA
ENST00000646753.1:c.1024+26_1024+29delinsTCAA	ENSP00000494065.1:n.1024+26_1024+29delinsTCAA
ENST00000267415.11:c.1129+26_1129+29delinsTCAA	ENSP00000267415.7:n.1129+26_1129+29delinsTCAA
ENST00000399423.8:c.*178_*181delinsTCAA	ENSP00000382350.4:n.*178_*181delinsTCAA
ENST00000557915.1:n.336+26_336+29delinsTCAA
ENST00000558566.1:c.*615_*618delinsTCAA	ENSP00000453025.1:n.*615_*618delinsTCAA
ENST00000558703.1:n.6_9delinsTCAA
ENST00000559969.5:c.1001_1004delinsTCAA
ENST00000560019.5:c.124+26_124+29delinsTCAA	ENSP00000453113.1:n.124+26_124+29delinsTCAA
ENST00000626689.2:c.*501+26_*501+29delinsTCAA	ENSP00000486681.1:n.*501+26_*501+29delinsTCAA
NM_001099274.1:c.1129+26_1129+29delinsTCAA	NP_001092744.1:n.1129+26_1129+29delinsTCAA
NM_012461.2:c.*178_*181delinsTCAA	NP_036593.2:n.*178_*181delinsTCAA
XM_005267528.2:c.1129+26_1129+29delinsTCAA	XP_005267585.1:n.1129+26_1129+29delinsTCAA
XM_005267529.2:c.1024+26_1024+29delinsTCAA	XP_005267586.1:n.1024+26_1024+29delinsTCAA
NM_001099274.2:c.1129+26_1129+29delinsTCAA	NP_001092744.1:n.1129+26_1129+29delinsTCAA
NM_001363668.1:c.1024+26_1024+29delinsTCAA	NP_001350597.1:n.1024+26_1024+29delinsTCAA
NM_012461.3:c.*178_*181delinsTCAA	NP_036593.2:n.*178_*181delinsTCAA
XM_011536642.2:c.*623_*626delinsTCAA	XP_011534944.1:n.*623_*626delinsTCAA
XM_017021216.2:c.487+26_487+29delinsTCAA	XP_016876705.1:n.487+26_487+29delinsTCAA
XM_017021217.1:c.487+26_487+29delinsTCAA	XP_016876706.1:n.487+26_487+29delinsTCAA
NM_001099274.3:c.1129+26_1129+29delinsTCAA MANE Select	NP_001092744.1:n.1129+26_1129+29delinsTCAA
NM_001363668.2:c.1024+26_1024+29delinsTCAA	NP_001350597.1:n.1024+26_1024+29delinsTCAA