Canonical Allele Identifier: CA485782137

Gene: TINF2

Linked Data

• COSMIC: COSM5104776
• MyVariant Identifiers: chr14:g.24709840G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240634G>T , CM000676.2:g.24240634G>T	GRCh38
NC_000014.8:g.24709840G>T , CM000676.1:g.24709840G>T	GRCh37
NC_000014.7:g.23779680G>T	NCBI36
NG_016650.1:g.7041C>A
NG_054634.1:g.13218G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1149C>A
ENST00000557921.3:c.738C>A	ENSP00000453157.3:p.Arg246=
ENST00000699682.1:n.1236C>A
ENST00000699683.1:n.1286C>A
ENST00000699684.1:c.*439C>A	ENSP00000514523.1:n.*439C>A
ENST00000699685.1:n.1050C>A
ENST00000699686.1:c.639C>A	ENSP00000514524.1:p.Arg213=
ENST00000699687.1:c.741C>A	ENSP00000514525.1:p.Arg247=
ENST00000699688.1:n.1046C>A
ENST00000699689.1:n.1402C>A
ENST00000699690.1:n.1599C>A
ENST00000699691.1:n.1743C>A
ENST00000699693.1:n.1263C>A
ENST00000699694.1:n.1505C>A
ENST00000699695.1:c.*218C>A	ENSP00000514526.1:n.*218C>A
ENST00000699696.1:n.1149C>A
ENST00000699697.1:c.846C>A	ENSP00000514527.1:p.Arg282=
ENST00000699698.1:n.767C>A
ENST00000699699.1:n.1170C>A
ENST00000699700.1:n.1293C>A
ENST00000699701.1:c.*226C>A	ENSP00000514528.1:n.*226C>A
ENST00000267415.12:c.846C>A MANE Select	ENSP00000267415.7:p.Arg282=
ENST00000557921.2:c.738C>A	ENSP00000453157.2:p.Arg246=
ENST00000646753.1:c.741C>A	ENSP00000494065.1:p.Arg247=
ENST00000267415.11:c.846C>A	ENSP00000267415.7:p.Arg282=
ENST00000399423.8:c.846C>A	ENSP00000382350.4:p.Arg282=
ENST00000558476.5:c.408C>A	ENSP00000452724.1:p.Arg136=
ENST00000558566.1:c.*218C>A	ENSP00000453025.1:n.*218C>A
ENST00000559019.1:c.*218C>A	ENSP00000453675.1:n.*218C>A
ENST00000559549.1:n.572C>A
ENST00000559969.5:c.757+45C>A
ENST00000626689.2:c.*218C>A	ENSP00000486681.1:n.*218C>A
NM_001099274.1:c.846C>A	NP_001092744.1:p.Arg282=
NM_012461.2:c.846C>A	NP_036593.2:p.Arg282=
XM_005267528.2:c.846C>A	XP_005267585.1:p.Arg282=
XM_005267529.2:c.741C>A	XP_005267586.1:p.Arg247=
NM_001099274.2:c.846C>A	NP_001092744.1:p.Arg282=
NM_001363668.1:c.741C>A	NP_001350597.1:p.Arg247=
NM_012461.3:c.846C>A	NP_036593.2:p.Arg282=
XM_011536642.2:c.*226C>A	XP_011534944.1:n.*226C>A
XM_017021216.2:c.204C>A	XP_016876705.1:p.Arg68=
XM_017021217.1:c.204C>A	XP_016876706.1:p.Arg68=
NM_001099274.3:c.846C>A MANE Select	NP_001092744.1:p.Arg282=
NM_001363668.2:c.741C>A	NP_001350597.1:p.Arg247=