Canonical Allele Identifier: CA485782158

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709860T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240654T>G , CM000676.2:g.24240654T>G	GRCh38
NC_000014.8:g.24709860T>G , CM000676.1:g.24709860T>G	GRCh37
NC_000014.7:g.23779700T>G	NCBI36
NG_016650.1:g.7021A>C
NG_054634.1:g.13238T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1129A>C
ENST00000557921.3:c.718A>C	ENSP00000453157.3:p.Arg240=
ENST00000699682.1:n.1216A>C
ENST00000699683.1:n.1266A>C
ENST00000699684.1:c.*419A>C	ENSP00000514523.1:n.*419A>C
ENST00000699685.1:n.1030A>C
ENST00000699686.1:c.619A>C	ENSP00000514524.1:p.Arg207=
ENST00000699687.1:c.721A>C	ENSP00000514525.1:p.Arg241=
ENST00000699688.1:n.1026A>C
ENST00000699689.1:n.1382A>C
ENST00000699690.1:n.1579A>C
ENST00000699691.1:n.1723A>C
ENST00000699693.1:n.1243A>C
ENST00000699694.1:n.1485A>C
ENST00000699695.1:c.*198A>C	ENSP00000514526.1:n.*198A>C
ENST00000699696.1:n.1129A>C
ENST00000699697.1:c.826A>C	ENSP00000514527.1:p.Arg276=
ENST00000699698.1:n.747A>C
ENST00000699699.1:n.1150A>C
ENST00000699700.1:n.1273A>C
ENST00000699701.1:c.*206A>C	ENSP00000514528.1:n.*206A>C
ENST00000267415.12:c.826A>C MANE Select	ENSP00000267415.7:p.Arg276=
ENST00000557921.2:c.718A>C	ENSP00000453157.2:p.Arg240=
ENST00000646753.1:c.721A>C	ENSP00000494065.1:p.Arg241=
ENST00000267415.11:c.826A>C	ENSP00000267415.7:p.Arg276=
ENST00000399423.8:c.826A>C	ENSP00000382350.4:p.Arg276=
ENST00000558476.5:c.388A>C	ENSP00000452724.1:p.Arg130=
ENST00000558566.1:c.*198A>C	ENSP00000453025.1:n.*198A>C
ENST00000559019.1:c.*198A>C	ENSP00000453675.1:n.*198A>C
ENST00000559549.1:n.552A>C
ENST00000559969.5:c.757+25A>C
ENST00000626689.2:c.*198A>C	ENSP00000486681.1:n.*198A>C
NM_001099274.1:c.826A>C	NP_001092744.1:p.Arg276=
NM_012461.2:c.826A>C	NP_036593.2:p.Arg276=
XM_005267528.2:c.826A>C	XP_005267585.1:p.Arg276=
XM_005267529.2:c.721A>C	XP_005267586.1:p.Arg241=
NM_001099274.2:c.826A>C	NP_001092744.1:p.Arg276=
NM_001363668.1:c.721A>C	NP_001350597.1:p.Arg241=
NM_012461.3:c.826A>C	NP_036593.2:p.Arg276=
XM_011536642.2:c.*206A>C	XP_011534944.1:n.*206A>C
XM_017021216.2:c.184A>C	XP_016876705.1:p.Arg62=
XM_017021217.1:c.184A>C	XP_016876706.1:p.Arg62=
NM_001099274.3:c.826A>C MANE Select	NP_001092744.1:p.Arg276=
NM_001363668.2:c.721A>C	NP_001350597.1:p.Arg241=