Canonical Allele Identifier: CA485782267

Gene: TINF2

Linked Data

• COSMIC: COSM5126736
• MyVariant Identifiers: chr14:g.24709921G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240715G>A , CM000676.2:g.24240715G>A	GRCh38
NC_000014.8:g.24709921G>A , CM000676.1:g.24709921G>A	GRCh37
NC_000014.7:g.23779761G>A	NCBI36
NG_016650.1:g.6960C>T
NG_054634.1:g.13299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1068C>T
ENST00000557921.3:c.657C>T	ENSP00000453157.3:p.Gly219=
ENST00000699682.1:n.1155C>T
ENST00000699683.1:n.1205C>T
ENST00000699684.1:c.*358C>T	ENSP00000514523.1:n.*358C>T
ENST00000699685.1:n.969C>T
ENST00000699686.1:c.558C>T	ENSP00000514524.1:p.Gly186=
ENST00000699687.1:c.660C>T	ENSP00000514525.1:p.Gly220=
ENST00000699688.1:n.965C>T
ENST00000699689.1:n.1321C>T
ENST00000699690.1:n.1518C>T
ENST00000699691.1:n.1662C>T
ENST00000699693.1:n.1182C>T
ENST00000699694.1:n.1424C>T
ENST00000699695.1:c.*137C>T	ENSP00000514526.1:n.*137C>T
ENST00000699696.1:n.1068C>T
ENST00000699697.1:c.765C>T	ENSP00000514527.1:p.Gly255=
ENST00000699698.1:n.686C>T
ENST00000699699.1:n.1089C>T
ENST00000699700.1:n.1212C>T
ENST00000699701.1:c.*145C>T	ENSP00000514528.1:n.*145C>T
ENST00000267415.12:c.765C>T MANE Select	ENSP00000267415.7:p.Gly255=
ENST00000557921.2:c.657C>T	ENSP00000453157.2:p.Gly219=
ENST00000646753.1:c.660C>T	ENSP00000494065.1:p.Gly220=
ENST00000267415.11:c.765C>T	ENSP00000267415.7:p.Gly255=
ENST00000399423.8:c.765C>T	ENSP00000382350.4:p.Gly255=
ENST00000558476.5:c.327C>T	ENSP00000452724.1:p.Gly109=
ENST00000558566.1:c.*137C>T	ENSP00000453025.1:n.*137C>T
ENST00000559019.1:c.*137C>T	ENSP00000453675.1:n.*137C>T
ENST00000559549.1:n.491C>T
ENST00000559969.5:c.721C>T
ENST00000626689.2:c.*137C>T	ENSP00000486681.1:n.*137C>T
NM_001099274.1:c.765C>T	NP_001092744.1:p.Gly255=
NM_012461.2:c.765C>T	NP_036593.2:p.Gly255=
XM_005267528.2:c.765C>T	XP_005267585.1:p.Gly255=
XM_005267529.2:c.660C>T	XP_005267586.1:p.Gly220=
NM_001099274.2:c.765C>T	NP_001092744.1:p.Gly255=
NM_001363668.1:c.660C>T	NP_001350597.1:p.Gly220=
NM_012461.3:c.765C>T	NP_036593.2:p.Gly255=
XM_011536642.2:c.*145C>T	XP_011534944.1:n.*145C>T
XM_017021216.2:c.123C>T	XP_016876705.1:p.Gly41=
XM_017021217.1:c.123C>T	XP_016876706.1:p.Gly41=
NM_001099274.3:c.765C>T MANE Select	NP_001092744.1:p.Gly255=
NM_001363668.2:c.660C>T	NP_001350597.1:p.Gly220=