Canonical Allele Identifier: CA2123849281

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240582T= , CM000676.2:g.24240582T=	GRCh38
NC_000014.8:g.24709788T= , CM000676.1:g.24709788T=	GRCh37
NC_000014.7:g.23779628T=	NCBI36
NG_016650.1:g.7093A=
NG_054634.1:g.13166T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1201A=
ENST00000557921.3:c.790A=	ENSP00000453157.3:p.Ile264=
ENST00000699682.1:n.1288A=
ENST00000699683.1:n.1338A=
ENST00000699684.1:c.*491A=	ENSP00000514523.1:n.*491A=
ENST00000699685.1:n.1102A=
ENST00000699686.1:c.691A=	ENSP00000514524.1:p.Ile231=
ENST00000699687.1:c.793A=	ENSP00000514525.1:p.Ile265=
ENST00000699688.1:n.1098A=
ENST00000699689.1:n.1454A=
ENST00000699690.1:n.1651A=
ENST00000699691.1:n.1795A=
ENST00000699693.1:n.1315A=
ENST00000699694.1:n.1557A=
ENST00000699695.1:c.*270A=	ENSP00000514526.1:n.*270A=
ENST00000699696.1:n.1201A=
ENST00000699697.1:c.898A=	ENSP00000514527.1:p.Ile300=
ENST00000699698.1:n.819A=
ENST00000699699.1:n.1222A=
ENST00000699700.1:n.1345A=
ENST00000699701.1:c.*278A=	ENSP00000514528.1:n.*278A=
ENST00000267415.12:c.898A= MANE Select	ENSP00000267415.7:p.Ile300=
ENST00000557921.2:c.790A=	ENSP00000453157.2:p.Ile264=
ENST00000646753.1:c.793A=	ENSP00000494065.1:p.Ile265=
ENST00000267415.11:c.898A=	ENSP00000267415.7:p.Ile300=
ENST00000399423.8:c.898A=	ENSP00000382350.4:p.Ile300=
ENST00000557915.1:n.17A=
ENST00000558566.1:c.*270A=	ENSP00000453025.1:n.*270A=
ENST00000559019.1:c.*270A=	ENSP00000453675.1:n.*270A=
ENST00000559549.1:n.624A=
ENST00000559969.5:c.757+97A=
ENST00000626689.2:c.*270A=	ENSP00000486681.1:n.*270A=
NM_001099274.1:c.898A=	NP_001092744.1:p.Ile300=
NM_012461.2:c.898A=	NP_036593.2:p.Ile300=
XM_005267528.2:c.898A=	XP_005267585.1:p.Ile300=
XM_005267529.2:c.793A=	XP_005267586.1:p.Ile265=
NM_001099274.2:c.898A=	NP_001092744.1:p.Ile300=
NM_001363668.1:c.793A=	NP_001350597.1:p.Ile265=
NM_012461.3:c.898A=	NP_036593.2:p.Ile300=
XM_011536642.2:c.*278A=	XP_011534944.1:n.*278A=
XM_017021216.2:c.256A=	XP_016876705.1:p.Ile86=
XM_017021217.1:c.256A=	XP_016876706.1:p.Ile86=
NM_001099274.3:c.898A= MANE Select	NP_001092744.1:p.Ile300=
NM_001363668.2:c.793A=	NP_001350597.1:p.Ile265=