Canonical Allele Identifier: CA485782217

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709893G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240687G>T , CM000676.2:g.24240687G>T	GRCh38
NC_000014.8:g.24709893G>T , CM000676.1:g.24709893G>T	GRCh37
NC_000014.7:g.23779733G>T	NCBI36
NG_016650.1:g.6988C>A
NG_054634.1:g.13271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1096C>A
ENST00000557921.3:c.685C>A	ENSP00000453157.3:p.Arg229=
ENST00000699682.1:n.1183C>A
ENST00000699683.1:n.1233C>A
ENST00000699684.1:c.*386C>A	ENSP00000514523.1:n.*386C>A
ENST00000699685.1:n.997C>A
ENST00000699686.1:c.586C>A	ENSP00000514524.1:p.Arg196=
ENST00000699687.1:c.688C>A	ENSP00000514525.1:p.Arg230=
ENST00000699688.1:n.993C>A
ENST00000699689.1:n.1349C>A
ENST00000699690.1:n.1546C>A
ENST00000699691.1:n.1690C>A
ENST00000699693.1:n.1210C>A
ENST00000699694.1:n.1452C>A
ENST00000699695.1:c.*165C>A	ENSP00000514526.1:n.*165C>A
ENST00000699696.1:n.1096C>A
ENST00000699697.1:c.793C>A	ENSP00000514527.1:p.Arg265=
ENST00000699698.1:n.714C>A
ENST00000699699.1:n.1117C>A
ENST00000699700.1:n.1240C>A
ENST00000699701.1:c.*173C>A	ENSP00000514528.1:n.*173C>A
ENST00000267415.12:c.793C>A MANE Select	ENSP00000267415.7:p.Arg265=
ENST00000557921.2:c.685C>A	ENSP00000453157.2:p.Arg229=
ENST00000646753.1:c.688C>A	ENSP00000494065.1:p.Arg230=
ENST00000267415.11:c.793C>A	ENSP00000267415.7:p.Arg265=
ENST00000399423.8:c.793C>A	ENSP00000382350.4:p.Arg265=
ENST00000558476.5:c.355C>A	ENSP00000452724.1:p.Arg119=
ENST00000558566.1:c.*165C>A	ENSP00000453025.1:n.*165C>A
ENST00000559019.1:c.*165C>A	ENSP00000453675.1:n.*165C>A
ENST00000559549.1:n.519C>A
ENST00000559969.5:c.749C>A
ENST00000626689.2:c.*165C>A	ENSP00000486681.1:n.*165C>A
NM_001099274.1:c.793C>A	NP_001092744.1:p.Arg265=
NM_012461.2:c.793C>A	NP_036593.2:p.Arg265=
XM_005267528.2:c.793C>A	XP_005267585.1:p.Arg265=
XM_005267529.2:c.688C>A	XP_005267586.1:p.Arg230=
NM_001099274.2:c.793C>A	NP_001092744.1:p.Arg265=
NM_001363668.1:c.688C>A	NP_001350597.1:p.Arg230=
NM_012461.3:c.793C>A	NP_036593.2:p.Arg265=
XM_011536642.2:c.*173C>A	XP_011534944.1:n.*173C>A
XM_017021216.2:c.151C>A	XP_016876705.1:p.Arg51=
XM_017021217.1:c.151C>A	XP_016876706.1:p.Arg51=
NM_001099274.3:c.793C>A MANE Select	NP_001092744.1:p.Arg265=
NM_001363668.2:c.688C>A	NP_001350597.1:p.Arg230=