Canonical Allele Identifier: CA485782143

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709636T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240430T>G , CM000676.2:g.24240430T>G	GRCh38
NC_000014.8:g.24709636T>G , CM000676.1:g.24709636T>G	GRCh37
NC_000014.7:g.23779476T>G	NCBI36
NG_016650.1:g.7245A>C
NG_054634.1:g.13014T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1353A>C
ENST00000557921.3:c.942A>C	ENSP00000453157.3:p.Thr314=
ENST00000699682.1:n.1440A>C
ENST00000699683.1:n.1490A>C
ENST00000699684.1:c.*643A>C	ENSP00000514523.1:n.*643A>C
ENST00000699685.1:n.1254A>C
ENST00000699686.1:c.843A>C	ENSP00000514524.1:p.Thr281=
ENST00000699687.1:c.945A>C	ENSP00000514525.1:p.Thr315=
ENST00000699688.1:n.1250A>C
ENST00000699689.1:n.1606A>C
ENST00000699690.1:n.1803A>C
ENST00000699691.1:n.1947A>C
ENST00000699693.1:n.1467A>C
ENST00000699694.1:n.1709A>C
ENST00000699695.1:c.*422A>C	ENSP00000514526.1:n.*422A>C
ENST00000699696.1:n.1353A>C
ENST00000699697.1:c.1050A>C	ENSP00000514527.1:p.Thr350=
ENST00000699698.1:n.971A>C
ENST00000699699.1:n.1374A>C
ENST00000699700.1:n.1497A>C
ENST00000699701.1:c.*430A>C	ENSP00000514528.1:n.*430A>C
ENST00000267415.12:c.1050A>C MANE Select	ENSP00000267415.7:p.Thr350=
ENST00000646753.1:c.945A>C	ENSP00000494065.1:p.Thr315=
ENST00000267415.11:c.1050A>C	ENSP00000267415.7:p.Thr350=
ENST00000399423.8:c.1050A>C	ENSP00000382350.4:p.Thr350=
ENST00000557915.1:n.169A>C
ENST00000558566.1:c.*422A>C	ENSP00000453025.1:n.*422A>C
ENST00000559969.5:c.808A>C
ENST00000560019.5:c.45A>C	ENSP00000453113.1:p.Thr15=
ENST00000626689.2:c.*422A>C	ENSP00000486681.1:n.*422A>C
NM_001099274.1:c.1050A>C	NP_001092744.1:p.Thr350=
NM_012461.2:c.1050A>C	NP_036593.2:p.Thr350=
XM_005267528.2:c.1050A>C	XP_005267585.1:p.Thr350=
XM_005267529.2:c.945A>C	XP_005267586.1:p.Thr315=
NM_001099274.2:c.1050A>C	NP_001092744.1:p.Thr350=
NM_001363668.1:c.945A>C	NP_001350597.1:p.Thr315=
NM_012461.3:c.1050A>C	NP_036593.2:p.Thr350=
XM_011536642.2:c.*430A>C	XP_011534944.1:n.*430A>C
XM_017021216.2:c.408A>C	XP_016876705.1:p.Thr136=
XM_017021217.1:c.408A>C	XP_016876706.1:p.Thr136=
NM_001099274.3:c.1050A>C MANE Select	NP_001092744.1:p.Thr350=
NM_001363668.2:c.945A>C	NP_001350597.1:p.Thr315=