Canonical Allele Identifier: CA2841381808

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240495dup , CM000676.2:g.24240495dup	GRCh38
NC_000014.8:g.24709701dup , CM000676.1:g.24709701dup	GRCh37
NC_000014.7:g.23779541dup	NCBI36
NG_016650.1:g.7181dup
NG_054634.1:g.13079dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1289dup
ENST00000557921.3:c.878dup	ENSP00000453157.3:p.Ser294GlufsTer17
ENST00000699682.1:n.1376dup
ENST00000699683.1:n.1426dup
ENST00000699684.1:c.*579dup	ENSP00000514523.1:n.*579dup
ENST00000699685.1:n.1190dup
ENST00000699686.1:c.779dup	ENSP00000514524.1:p.Ser261GlufsTer17
ENST00000699687.1:c.881dup	ENSP00000514525.1:p.Ser295GlufsTer17
ENST00000699688.1:n.1186dup
ENST00000699689.1:n.1542dup
ENST00000699690.1:n.1739dup
ENST00000699691.1:n.1883dup
ENST00000699693.1:n.1403dup
ENST00000699694.1:n.1645dup
ENST00000699695.1:c.*358dup	ENSP00000514526.1:n.*358dup
ENST00000699696.1:n.1289dup
ENST00000699697.1:c.986dup	ENSP00000514527.1:p.Ser330GlufsTer17
ENST00000699698.1:n.907dup
ENST00000699699.1:n.1310dup
ENST00000699700.1:n.1433dup
ENST00000699701.1:c.*366dup	ENSP00000514528.1:n.*366dup
ENST00000267415.12:c.986dup MANE Select	ENSP00000267415.7:p.Ser330GlufsTer17
ENST00000646753.1:c.881dup	ENSP00000494065.1:p.Ser295GlufsTer17
ENST00000267415.11:c.986dup	ENSP00000267415.7:p.Ser330GlufsTer17
ENST00000399423.8:c.986dup	ENSP00000382350.4:p.Ser330GlufsTer17
ENST00000557915.1:n.105dup
ENST00000558566.1:c.*358dup	ENSP00000453025.1:n.*358dup
ENST00000559019.1:c.*358dup	ENSP00000453675.1:n.*358dup
ENST00000559969.5:c.758-14dup
ENST00000626689.2:c.*358dup	ENSP00000486681.1:n.*358dup
NM_001099274.1:c.986dup	NP_001092744.1:p.Ser330GlufsTer17
NM_012461.2:c.986dup	NP_036593.2:p.Ser330GlufsTer17
XM_005267528.2:c.986dup	XP_005267585.1:p.Ser330GlufsTer17
XM_005267529.2:c.881dup	XP_005267586.1:p.Ser295GlufsTer17
NM_001099274.2:c.986dup	NP_001092744.1:p.Ser330GlufsTer17
NM_001363668.1:c.881dup	NP_001350597.1:p.Ser295GlufsTer17
NM_012461.3:c.986dup	NP_036593.2:p.Ser330GlufsTer17
XM_011536642.2:c.*366dup	XP_011534944.1:n.*366dup
XM_017021216.2:c.344dup	XP_016876705.1:p.Ser116GlufsTer17
XM_017021217.1:c.344dup	XP_016876706.1:p.Ser116GlufsTer17
NM_001099274.3:c.986dup MANE Select	NP_001092744.1:p.Ser330GlufsTer17
NM_001363668.2:c.881dup	NP_001350597.1:p.Ser295GlufsTer17