Canonical Allele Identifier: CA2695213967

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240623delinsGC , CM000676.2:g.24240623delinsGC	GRCh38
NC_000014.8:g.24709829delinsGC , CM000676.1:g.24709829delinsGC	GRCh37
NC_000014.7:g.23779669delinsGC	NCBI36
NG_016650.1:g.7052delinsGC
NG_054634.1:g.13207delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1160delinsGC
ENST00000557921.3:c.749delinsGC	ENSP00000453157.3:p.Met250SerfsTer6
ENST00000699682.1:n.1247delinsGC
ENST00000699683.1:n.1297delinsGC
ENST00000699684.1:c.*450delinsGC	ENSP00000514523.1:n.*450delinsGC
ENST00000699685.1:n.1061delinsGC
ENST00000699686.1:c.650delinsGC	ENSP00000514524.1:p.Met217SerfsTer6
ENST00000699687.1:c.752delinsGC	ENSP00000514525.1:p.Met251SerfsTer6
ENST00000699688.1:n.1057delinsGC
ENST00000699689.1:n.1413delinsGC
ENST00000699690.1:n.1610delinsGC
ENST00000699691.1:n.1754delinsGC
ENST00000699693.1:n.1274delinsGC
ENST00000699694.1:n.1516delinsGC
ENST00000699695.1:c.*229delinsGC	ENSP00000514526.1:n.*229delinsGC
ENST00000699696.1:n.1160delinsGC
ENST00000699697.1:c.857delinsGC	ENSP00000514527.1:p.Met286SerfsTer6
ENST00000699698.1:n.778delinsGC
ENST00000699699.1:n.1181delinsGC
ENST00000699700.1:n.1304delinsGC
ENST00000699701.1:c.*237delinsGC	ENSP00000514528.1:n.*237delinsGC
ENST00000267415.12:c.857delinsGC MANE Select	ENSP00000267415.7:p.Met286SerfsTer6
ENST00000557921.2:c.749delinsGC	ENSP00000453157.2:p.Met250SerfsTer6
ENST00000646753.1:c.752delinsGC	ENSP00000494065.1:p.Met251SerfsTer6
ENST00000267415.11:c.857delinsGC	ENSP00000267415.7:p.Met286SerfsTer6
ENST00000399423.8:c.857delinsGC	ENSP00000382350.4:p.Met286SerfsTer6
ENST00000558476.5:c.419delinsGC	ENSP00000452724.1:p.Met140SerfsTer6
ENST00000558566.1:c.*229delinsGC	ENSP00000453025.1:n.*229delinsGC
ENST00000559019.1:c.*229delinsGC	ENSP00000453675.1:n.*229delinsGC
ENST00000559549.1:n.583delinsGC
ENST00000559969.5:c.757+56delinsGC
ENST00000626689.2:c.*229delinsGC	ENSP00000486681.1:n.*229delinsGC
NM_001099274.1:c.857delinsGC	NP_001092744.1:p.Met286SerfsTer6
NM_012461.2:c.857delinsGC	NP_036593.2:p.Met286SerfsTer6
XM_005267528.2:c.857delinsGC	XP_005267585.1:p.Met286SerfsTer6
XM_005267529.2:c.752delinsGC	XP_005267586.1:p.Met251SerfsTer6
NM_001099274.2:c.857delinsGC	NP_001092744.1:p.Met286SerfsTer6
NM_001363668.1:c.752delinsGC	NP_001350597.1:p.Met251SerfsTer6
NM_012461.3:c.857delinsGC	NP_036593.2:p.Met286SerfsTer6
XM_011536642.2:c.*237delinsGC	XP_011534944.1:n.*237delinsGC
XM_017021216.2:c.215delinsGC	XP_016876705.1:p.Met72SerfsTer6
XM_017021217.1:c.215delinsGC	XP_016876706.1:p.Met72SerfsTer6
NM_001099274.3:c.857delinsGC MANE Select	NP_001092744.1:p.Met286SerfsTer6
NM_001363668.2:c.752delinsGC	NP_001350597.1:p.Met251SerfsTer6