Canonical Allele Identifier: CA389224137

Gene: TINF2

Linked Data

• COSMIC: COSM954973 ; COSM1587354
• MyVariant Identifiers: chr14:g.24709719C>T (hg19) ; chr14:g.24240513C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240513C>T , CM000676.2:g.24240513C>T	GRCh38
NC_000014.8:g.24709719C>T , CM000676.1:g.24709719C>T	GRCh37
NC_000014.7:g.23779559C>T	NCBI36
NG_016650.1:g.7162G>A
NG_054634.1:g.13097C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1270G>A
ENST00000557921.3:c.859G>A	ENSP00000453157.3:p.Ala287Thr
ENST00000699682.1:n.1357G>A
ENST00000699683.1:n.1407G>A
ENST00000699684.1:c.*560G>A	ENSP00000514523.1:n.*560G>A
ENST00000699685.1:n.1171G>A
ENST00000699686.1:c.760G>A	ENSP00000514524.1:p.Ala254Thr
ENST00000699687.1:c.862G>A	ENSP00000514525.1:p.Ala288Thr
ENST00000699688.1:n.1167G>A
ENST00000699689.1:n.1523G>A
ENST00000699690.1:n.1720G>A
ENST00000699691.1:n.1864G>A
ENST00000699693.1:n.1384G>A
ENST00000699694.1:n.1626G>A
ENST00000699695.1:c.*339G>A	ENSP00000514526.1:n.*339G>A
ENST00000699696.1:n.1270G>A
ENST00000699697.1:c.967G>A	ENSP00000514527.1:p.Ala323Thr
ENST00000699698.1:n.888G>A
ENST00000699699.1:n.1291G>A
ENST00000699700.1:n.1414G>A
ENST00000699701.1:c.*347G>A	ENSP00000514528.1:n.*347G>A
ENST00000267415.12:c.967G>A MANE Select	ENSP00000267415.7:p.Ala323Thr
ENST00000557921.2:c.859G>A	ENSP00000453157.2:p.Ala287Thr
ENST00000646753.1:c.862G>A	ENSP00000494065.1:p.Ala288Thr
ENST00000267415.11:c.967G>A	ENSP00000267415.7:p.Ala323Thr
ENST00000399423.8:c.967G>A	ENSP00000382350.4:p.Ala323Thr
ENST00000557915.1:n.86G>A
ENST00000558566.1:c.*339G>A	ENSP00000453025.1:n.*339G>A
ENST00000559019.1:c.*339G>A	ENSP00000453675.1:n.*339G>A
ENST00000559969.5:c.758-33G>A
ENST00000626689.2:c.*339G>A	ENSP00000486681.1:n.*339G>A
NM_001099274.1:c.967G>A	NP_001092744.1:p.Ala323Thr
NM_012461.2:c.967G>A	NP_036593.2:p.Ala323Thr
XM_005267528.2:c.967G>A	XP_005267585.1:p.Ala323Thr
XM_005267529.2:c.862G>A	XP_005267586.1:p.Ala288Thr
NM_001099274.2:c.967G>A	NP_001092744.1:p.Ala323Thr
NM_001363668.1:c.862G>A	NP_001350597.1:p.Ala288Thr
NM_012461.3:c.967G>A	NP_036593.2:p.Ala323Thr
XM_011536642.2:c.*347G>A	XP_011534944.1:n.*347G>A
XM_017021216.2:c.325G>A	XP_016876705.1:p.Ala109Thr
XM_017021217.1:c.325G>A	XP_016876706.1:p.Ala109Thr
NM_001099274.3:c.967G>A MANE Select	NP_001092744.1:p.Ala323Thr
NM_001363668.2:c.862G>A	NP_001350597.1:p.Ala288Thr