Canonical Allele Identifier: CA2123849282

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240584A= , CM000676.2:g.24240584A=	GRCh38
NC_000014.8:g.24709790A= , CM000676.1:g.24709790A=	GRCh37
NC_000014.7:g.23779630A=	NCBI36
NG_016650.1:g.7091T=
NG_054634.1:g.13168A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1199T=
ENST00000557921.3:c.788T=	ENSP00000453157.3:p.Val263=
ENST00000699682.1:n.1286T=
ENST00000699683.1:n.1336T=
ENST00000699684.1:c.*489T=	ENSP00000514523.1:n.*489T=
ENST00000699685.1:n.1100T=
ENST00000699686.1:c.689T=	ENSP00000514524.1:p.Val230=
ENST00000699687.1:c.791T=	ENSP00000514525.1:p.Val264=
ENST00000699688.1:n.1096T=
ENST00000699689.1:n.1452T=
ENST00000699690.1:n.1649T=
ENST00000699691.1:n.1793T=
ENST00000699693.1:n.1313T=
ENST00000699694.1:n.1555T=
ENST00000699695.1:c.*268T=	ENSP00000514526.1:n.*268T=
ENST00000699696.1:n.1199T=
ENST00000699697.1:c.896T=	ENSP00000514527.1:p.Val299=
ENST00000699698.1:n.817T=
ENST00000699699.1:n.1220T=
ENST00000699700.1:n.1343T=
ENST00000699701.1:c.*276T=	ENSP00000514528.1:n.*276T=
ENST00000267415.12:c.896T= MANE Select	ENSP00000267415.7:p.Val299=
ENST00000557921.2:c.788T=	ENSP00000453157.2:p.Val263=
ENST00000646753.1:c.791T=	ENSP00000494065.1:p.Val264=
ENST00000267415.11:c.896T=	ENSP00000267415.7:p.Val299=
ENST00000399423.8:c.896T=	ENSP00000382350.4:p.Val299=
ENST00000557915.1:n.15T=
ENST00000558566.1:c.*268T=	ENSP00000453025.1:n.*268T=
ENST00000559019.1:c.*268T=	ENSP00000453675.1:n.*268T=
ENST00000559549.1:n.622T=
ENST00000559969.5:c.757+95T=
ENST00000626689.2:c.*268T=	ENSP00000486681.1:n.*268T=
NM_001099274.1:c.896T=	NP_001092744.1:p.Val299=
NM_012461.2:c.896T=	NP_036593.2:p.Val299=
XM_005267528.2:c.896T=	XP_005267585.1:p.Val299=
XM_005267529.2:c.791T=	XP_005267586.1:p.Val264=
NM_001099274.2:c.896T=	NP_001092744.1:p.Val299=
NM_001363668.1:c.791T=	NP_001350597.1:p.Val264=
NM_012461.3:c.896T=	NP_036593.2:p.Val299=
XM_011536642.2:c.*276T=	XP_011534944.1:n.*276T=
XM_017021216.2:c.254T=	XP_016876705.1:p.Val85=
XM_017021217.1:c.254T=	XP_016876706.1:p.Val85=
NM_001099274.3:c.896T= MANE Select	NP_001092744.1:p.Val299=
NM_001363668.2:c.791T=	NP_001350597.1:p.Val264=