Canonical Allele Identifier: CA485782240

Gene: TINF2

Linked Data

• COSMIC: COSM5555319 ; COSM5555320
• MyVariant Identifiers: chr14:g.24709675T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240469T>C , CM000676.2:g.24240469T>C	GRCh38
NC_000014.8:g.24709675T>C , CM000676.1:g.24709675T>C	GRCh37
NC_000014.7:g.23779515T>C	NCBI36
NG_016650.1:g.7206A>G
NG_054634.1:g.13053T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1314A>G
ENST00000557921.3:c.903A>G	ENSP00000453157.3:p.Gly301=
ENST00000699682.1:n.1401A>G
ENST00000699683.1:n.1451A>G
ENST00000699684.1:c.*604A>G	ENSP00000514523.1:n.*604A>G
ENST00000699685.1:n.1215A>G
ENST00000699686.1:c.804A>G	ENSP00000514524.1:p.Gly268=
ENST00000699687.1:c.906A>G	ENSP00000514525.1:p.Gly302=
ENST00000699688.1:n.1211A>G
ENST00000699689.1:n.1567A>G
ENST00000699690.1:n.1764A>G
ENST00000699691.1:n.1908A>G
ENST00000699693.1:n.1428A>G
ENST00000699694.1:n.1670A>G
ENST00000699695.1:c.*383A>G	ENSP00000514526.1:n.*383A>G
ENST00000699696.1:n.1314A>G
ENST00000699697.1:c.1011A>G	ENSP00000514527.1:p.Gly337=
ENST00000699698.1:n.932A>G
ENST00000699699.1:n.1335A>G
ENST00000699700.1:n.1458A>G
ENST00000699701.1:c.*391A>G	ENSP00000514528.1:n.*391A>G
ENST00000267415.12:c.1011A>G MANE Select	ENSP00000267415.7:p.Gly337=
ENST00000646753.1:c.906A>G	ENSP00000494065.1:p.Gly302=
ENST00000267415.11:c.1011A>G	ENSP00000267415.7:p.Gly337=
ENST00000399423.8:c.1011A>G	ENSP00000382350.4:p.Gly337=
ENST00000557915.1:n.130A>G
ENST00000558566.1:c.*383A>G	ENSP00000453025.1:n.*383A>G
ENST00000559969.5:c.769A>G
ENST00000560019.5:c.6A>G	ENSP00000453113.1:p.Gly2=
ENST00000626689.2:c.*383A>G	ENSP00000486681.1:n.*383A>G
NM_001099274.1:c.1011A>G	NP_001092744.1:p.Gly337=
NM_012461.2:c.1011A>G	NP_036593.2:p.Gly337=
XM_005267528.2:c.1011A>G	XP_005267585.1:p.Gly337=
XM_005267529.2:c.906A>G	XP_005267586.1:p.Gly302=
NM_001099274.2:c.1011A>G	NP_001092744.1:p.Gly337=
NM_001363668.1:c.906A>G	NP_001350597.1:p.Gly302=
NM_012461.3:c.1011A>G	NP_036593.2:p.Gly337=
XM_011536642.2:c.*391A>G	XP_011534944.1:n.*391A>G
XM_017021216.2:c.369A>G	XP_016876705.1:p.Gly123=
XM_017021217.1:c.369A>G	XP_016876706.1:p.Gly123=
NM_001099274.3:c.1011A>G MANE Select	NP_001092744.1:p.Gly337=
NM_001363668.2:c.906A>G	NP_001350597.1:p.Gly302=