Canonical Allele Identifier: CA485782206

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709888T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240682T>C , CM000676.2:g.24240682T>C	GRCh38
NC_000014.8:g.24709888T>C , CM000676.1:g.24709888T>C	GRCh37
NC_000014.7:g.23779728T>C	NCBI36
NG_016650.1:g.6993A>G
NG_054634.1:g.13266T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1101A>G
ENST00000557921.3:c.690A>G	ENSP00000453157.3:p.Arg230=
ENST00000699682.1:n.1188A>G
ENST00000699683.1:n.1238A>G
ENST00000699684.1:c.*391A>G	ENSP00000514523.1:n.*391A>G
ENST00000699685.1:n.1002A>G
ENST00000699686.1:c.591A>G	ENSP00000514524.1:p.Arg197=
ENST00000699687.1:c.693A>G	ENSP00000514525.1:p.Arg231=
ENST00000699688.1:n.998A>G
ENST00000699689.1:n.1354A>G
ENST00000699690.1:n.1551A>G
ENST00000699691.1:n.1695A>G
ENST00000699693.1:n.1215A>G
ENST00000699694.1:n.1457A>G
ENST00000699695.1:c.*170A>G	ENSP00000514526.1:n.*170A>G
ENST00000699696.1:n.1101A>G
ENST00000699697.1:c.798A>G	ENSP00000514527.1:p.Arg266=
ENST00000699698.1:n.719A>G
ENST00000699699.1:n.1122A>G
ENST00000699700.1:n.1245A>G
ENST00000699701.1:c.*178A>G	ENSP00000514528.1:n.*178A>G
ENST00000267415.12:c.798A>G MANE Select	ENSP00000267415.7:p.Arg266=
ENST00000557921.2:c.690A>G	ENSP00000453157.2:p.Arg230=
ENST00000646753.1:c.693A>G	ENSP00000494065.1:p.Arg231=
ENST00000267415.11:c.798A>G	ENSP00000267415.7:p.Arg266=
ENST00000399423.8:c.798A>G	ENSP00000382350.4:p.Arg266=
ENST00000558476.5:c.360A>G	ENSP00000452724.1:p.Arg120=
ENST00000558566.1:c.*170A>G	ENSP00000453025.1:n.*170A>G
ENST00000559019.1:c.*170A>G	ENSP00000453675.1:n.*170A>G
ENST00000559549.1:n.524A>G
ENST00000559969.5:c.754A>G
ENST00000626689.2:c.*170A>G	ENSP00000486681.1:n.*170A>G
NM_001099274.1:c.798A>G	NP_001092744.1:p.Arg266=
NM_012461.2:c.798A>G	NP_036593.2:p.Arg266=
XM_005267528.2:c.798A>G	XP_005267585.1:p.Arg266=
XM_005267529.2:c.693A>G	XP_005267586.1:p.Arg231=
NM_001099274.2:c.798A>G	NP_001092744.1:p.Arg266=
NM_001363668.1:c.693A>G	NP_001350597.1:p.Arg231=
NM_012461.3:c.798A>G	NP_036593.2:p.Arg266=
XM_011536642.2:c.*178A>G	XP_011534944.1:n.*178A>G
XM_017021216.2:c.156A>G	XP_016876705.1:p.Arg52=
XM_017021217.1:c.156A>G	XP_016876706.1:p.Arg52=
NM_001099274.3:c.798A>G MANE Select	NP_001092744.1:p.Arg266=
NM_001363668.2:c.693A>G	NP_001350597.1:p.Arg231=