Canonical Allele Identifier: CA2841381809

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240784dup , CM000676.2:g.24240784dup	GRCh38
NC_000014.8:g.24709990dup , CM000676.1:g.24709990dup	GRCh37
NC_000014.7:g.23779830dup	NCBI36
NG_016650.1:g.6894dup
NG_054634.1:g.13368dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1002dup
ENST00000557921.3:c.591dup	ENSP00000453157.3:p.Ala198SerfsTer?
ENST00000699682.1:n.1089dup
ENST00000699683.1:n.1139dup
ENST00000699684.1:c.*292dup	ENSP00000514523.1:n.*292dup
ENST00000699685.1:n.903dup
ENST00000699686.1:c.492dup	ENSP00000514524.1:p.Ala165SerfsTer?
ENST00000699687.1:c.594dup	ENSP00000514525.1:p.Ala199SerfsTer?
ENST00000699688.1:n.899dup
ENST00000699689.1:n.1255dup
ENST00000699690.1:n.1452dup
ENST00000699691.1:n.1596dup
ENST00000699693.1:n.1116dup
ENST00000699694.1:n.1358dup
ENST00000699695.1:c.*71dup	ENSP00000514526.1:n.*71dup
ENST00000699696.1:n.1002dup
ENST00000699697.1:c.699dup	ENSP00000514527.1:p.Ala234SerfsTer?
ENST00000699698.1:n.620dup
ENST00000699699.1:n.1023dup
ENST00000699700.1:n.1146dup
ENST00000699701.1:c.*79dup	ENSP00000514528.1:n.*79dup
ENST00000267415.12:c.699dup MANE Select	ENSP00000267415.7:p.Ala234SerfsTer?
ENST00000557921.2:c.591dup	ENSP00000453157.2:p.Ala198SerfsTer?
ENST00000646753.1:c.594dup	ENSP00000494065.1:p.Ala199SerfsTer?
ENST00000267415.11:c.699dup	ENSP00000267415.7:p.Ala234SerfsTer?
ENST00000399423.8:c.699dup	ENSP00000382350.4:p.Ala234SerfsTer?
ENST00000558476.5:c.261dup	ENSP00000452724.1:p.Ala88SerfsTer?
ENST00000558566.1:c.*71dup	ENSP00000453025.1:n.*71dup
ENST00000559019.1:c.*71dup	ENSP00000453675.1:n.*71dup
ENST00000559549.1:n.425dup
ENST00000559969.5:c.655dup
ENST00000626689.2:c.*71dup	ENSP00000486681.1:n.*71dup
NM_001099274.1:c.699dup	NP_001092744.1:p.Ala234SerfsTer?
NM_012461.2:c.699dup	NP_036593.2:p.Ala234SerfsTer?
XM_005267528.2:c.699dup	XP_005267585.1:p.Ala234SerfsTer?
XM_005267529.2:c.594dup	XP_005267586.1:p.Ala199SerfsTer?
NM_001099274.2:c.699dup	NP_001092744.1:p.Ala234SerfsTer?
NM_001363668.1:c.594dup	NP_001350597.1:p.Ala199SerfsTer?
NM_012461.3:c.699dup	NP_036593.2:p.Ala234SerfsTer?
XM_011536642.2:c.*79dup	XP_011534944.1:n.*79dup
XM_017021216.2:c.57dup	XP_016876705.1:p.Ala20SerfsTer?
XM_017021217.1:c.57dup	XP_016876706.1:p.Ala20SerfsTer?
NM_001099274.3:c.699dup MANE Select	NP_001092744.1:p.Ala234SerfsTer?
NM_001363668.2:c.594dup	NP_001350597.1:p.Ala199SerfsTer?