Canonical Allele Identifier: CA2123849349

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240727T= , CM000676.2:g.24240727T=	GRCh38
NC_000014.8:g.24709933T= , CM000676.1:g.24709933T=	GRCh37
NC_000014.7:g.23779773T=	NCBI36
NG_016650.1:g.6948A=
NG_054634.1:g.13311T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1056A=
ENST00000557921.3:c.645A=	ENSP00000453157.3:p.Glu215=
ENST00000699682.1:n.1143A=
ENST00000699683.1:n.1193A=
ENST00000699684.1:c.*346A=	ENSP00000514523.1:n.*346A=
ENST00000699685.1:n.957A=
ENST00000699686.1:c.546A=	ENSP00000514524.1:p.Glu182=
ENST00000699687.1:c.648A=	ENSP00000514525.1:p.Glu216=
ENST00000699688.1:n.953A=
ENST00000699689.1:n.1309A=
ENST00000699690.1:n.1506A=
ENST00000699691.1:n.1650A=
ENST00000699693.1:n.1170A=
ENST00000699694.1:n.1412A=
ENST00000699695.1:c.*125A=	ENSP00000514526.1:n.*125A=
ENST00000699696.1:n.1056A=
ENST00000699697.1:c.753A=	ENSP00000514527.1:p.Glu251=
ENST00000699698.1:n.674A=
ENST00000699699.1:n.1077A=
ENST00000699700.1:n.1200A=
ENST00000699701.1:c.*133A=	ENSP00000514528.1:n.*133A=
ENST00000267415.12:c.753A= MANE Select	ENSP00000267415.7:p.Glu251=
ENST00000557921.2:c.645A=	ENSP00000453157.2:p.Glu215=
ENST00000646753.1:c.648A=	ENSP00000494065.1:p.Glu216=
ENST00000267415.11:c.753A=	ENSP00000267415.7:p.Glu251=
ENST00000399423.8:c.753A=	ENSP00000382350.4:p.Glu251=
ENST00000558476.5:c.315A=	ENSP00000452724.1:p.Glu105=
ENST00000558566.1:c.*125A=	ENSP00000453025.1:n.*125A=
ENST00000559019.1:c.*125A=	ENSP00000453675.1:n.*125A=
ENST00000559549.1:n.479A=
ENST00000559969.5:c.709A=
ENST00000626689.2:c.*125A=	ENSP00000486681.1:n.*125A=
NM_001099274.1:c.753A=	NP_001092744.1:p.Glu251=
NM_012461.2:c.753A=	NP_036593.2:p.Glu251=
XM_005267528.2:c.753A=	XP_005267585.1:p.Glu251=
XM_005267529.2:c.648A=	XP_005267586.1:p.Glu216=
NM_001099274.2:c.753A=	NP_001092744.1:p.Glu251=
NM_001363668.1:c.648A=	NP_001350597.1:p.Glu216=
NM_012461.3:c.753A=	NP_036593.2:p.Glu251=
XM_011536642.2:c.*133A=	XP_011534944.1:n.*133A=
XM_017021216.2:c.111A=	XP_016876705.1:p.Glu37=
XM_017021217.1:c.111A=	XP_016876706.1:p.Glu37=
NM_001099274.3:c.753A= MANE Select	NP_001092744.1:p.Glu251=
NM_001363668.2:c.648A=	NP_001350597.1:p.Glu216=