Canonical Allele Identifier: CA389226306

Gene: TINF2

Linked Data

• COSMIC: COSM267576 ; COSM267577
• MyVariant Identifiers: chr14:g.24709895C>T (hg19) ; chr14:g.24240689C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240689C>T , CM000676.2:g.24240689C>T	GRCh38
NC_000014.8:g.24709895C>T , CM000676.1:g.24709895C>T	GRCh37
NC_000014.7:g.23779735C>T	NCBI36
NG_016650.1:g.6986G>A
NG_054634.1:g.13273C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1094G>A
ENST00000557921.3:c.683G>A	ENSP00000453157.3:p.Gly228Asp
ENST00000699682.1:n.1181G>A
ENST00000699683.1:n.1231G>A
ENST00000699684.1:c.*384G>A	ENSP00000514523.1:n.*384G>A
ENST00000699685.1:n.995G>A
ENST00000699686.1:c.584G>A	ENSP00000514524.1:p.Gly195Asp
ENST00000699687.1:c.686G>A	ENSP00000514525.1:p.Gly229Asp
ENST00000699688.1:n.991G>A
ENST00000699689.1:n.1347G>A
ENST00000699690.1:n.1544G>A
ENST00000699691.1:n.1688G>A
ENST00000699693.1:n.1208G>A
ENST00000699694.1:n.1450G>A
ENST00000699695.1:c.*163G>A	ENSP00000514526.1:n.*163G>A
ENST00000699696.1:n.1094G>A
ENST00000699697.1:c.791G>A	ENSP00000514527.1:p.Gly264Asp
ENST00000699698.1:n.712G>A
ENST00000699699.1:n.1115G>A
ENST00000699700.1:n.1238G>A
ENST00000699701.1:c.*171G>A	ENSP00000514528.1:n.*171G>A
ENST00000267415.12:c.791G>A MANE Select	ENSP00000267415.7:p.Gly264Asp
ENST00000557921.2:c.683G>A	ENSP00000453157.2:p.Gly228Asp
ENST00000646753.1:c.686G>A	ENSP00000494065.1:p.Gly229Asp
ENST00000267415.11:c.791G>A	ENSP00000267415.7:p.Gly264Asp
ENST00000399423.8:c.791G>A	ENSP00000382350.4:p.Gly264Asp
ENST00000558476.5:c.353G>A	ENSP00000452724.1:p.Gly118Asp
ENST00000558566.1:c.*163G>A	ENSP00000453025.1:n.*163G>A
ENST00000559019.1:c.*163G>A	ENSP00000453675.1:n.*163G>A
ENST00000559549.1:n.517G>A
ENST00000559969.5:c.747G>A
ENST00000626689.2:c.*163G>A	ENSP00000486681.1:n.*163G>A
NM_001099274.1:c.791G>A	NP_001092744.1:p.Gly264Asp
NM_012461.2:c.791G>A	NP_036593.2:p.Gly264Asp
XM_005267528.2:c.791G>A	XP_005267585.1:p.Gly264Asp
XM_005267529.2:c.686G>A	XP_005267586.1:p.Gly229Asp
NM_001099274.2:c.791G>A	NP_001092744.1:p.Gly264Asp
NM_001363668.1:c.686G>A	NP_001350597.1:p.Gly229Asp
NM_012461.3:c.791G>A	NP_036593.2:p.Gly264Asp
XM_011536642.2:c.*171G>A	XP_011534944.1:n.*171G>A
XM_017021216.2:c.149G>A	XP_016876705.1:p.Gly50Asp
XM_017021217.1:c.149G>A	XP_016876706.1:p.Gly50Asp
NM_001099274.3:c.791G>A MANE Select	NP_001092744.1:p.Gly264Asp
NM_001363668.2:c.686G>A	NP_001350597.1:p.Gly229Asp