Canonical Allele Identifier: CA389225085

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709796G>C (hg19) ; chr14:g.24240590G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240590G>C , CM000676.2:g.24240590G>C	GRCh38
NC_000014.8:g.24709796G>C , CM000676.1:g.24709796G>C	GRCh37
NC_000014.7:g.23779636G>C	NCBI36
NG_016650.1:g.7085C>G
NG_054634.1:g.13174G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1193C>G
ENST00000557921.3:c.782C>G	ENSP00000453157.3:p.Thr261Ser
ENST00000699682.1:n.1280C>G
ENST00000699683.1:n.1330C>G
ENST00000699684.1:c.*483C>G	ENSP00000514523.1:n.*483C>G
ENST00000699685.1:n.1094C>G
ENST00000699686.1:c.683C>G	ENSP00000514524.1:p.Thr228Ser
ENST00000699687.1:c.785C>G	ENSP00000514525.1:p.Thr262Ser
ENST00000699688.1:n.1090C>G
ENST00000699689.1:n.1446C>G
ENST00000699690.1:n.1643C>G
ENST00000699691.1:n.1787C>G
ENST00000699693.1:n.1307C>G
ENST00000699694.1:n.1549C>G
ENST00000699695.1:c.*262C>G	ENSP00000514526.1:n.*262C>G
ENST00000699696.1:n.1193C>G
ENST00000699697.1:c.890C>G	ENSP00000514527.1:p.Thr297Ser
ENST00000699698.1:n.811C>G
ENST00000699699.1:n.1214C>G
ENST00000699700.1:n.1337C>G
ENST00000699701.1:c.*270C>G	ENSP00000514528.1:n.*270C>G
ENST00000267415.12:c.890C>G MANE Select	ENSP00000267415.7:p.Thr297Ser
ENST00000557921.2:c.782C>G	ENSP00000453157.2:p.Thr261Ser
ENST00000646753.1:c.785C>G	ENSP00000494065.1:p.Thr262Ser
ENST00000267415.11:c.890C>G	ENSP00000267415.7:p.Thr297Ser
ENST00000399423.8:c.890C>G	ENSP00000382350.4:p.Thr297Ser
ENST00000557915.1:n.9C>G
ENST00000558566.1:c.*262C>G	ENSP00000453025.1:n.*262C>G
ENST00000559019.1:c.*262C>G	ENSP00000453675.1:n.*262C>G
ENST00000559549.1:n.616C>G
ENST00000559969.5:c.757+89C>G
ENST00000626689.2:c.*262C>G	ENSP00000486681.1:n.*262C>G
NM_001099274.1:c.890C>G	NP_001092744.1:p.Thr297Ser
NM_012461.2:c.890C>G	NP_036593.2:p.Thr297Ser
XM_005267528.2:c.890C>G	XP_005267585.1:p.Thr297Ser
XM_005267529.2:c.785C>G	XP_005267586.1:p.Thr262Ser
NM_001099274.2:c.890C>G	NP_001092744.1:p.Thr297Ser
NM_001363668.1:c.785C>G	NP_001350597.1:p.Thr262Ser
NM_012461.3:c.890C>G	NP_036593.2:p.Thr297Ser
XM_011536642.2:c.*270C>G	XP_011534944.1:n.*270C>G
XM_017021216.2:c.248C>G	XP_016876705.1:p.Thr83Ser
XM_017021217.1:c.248C>G	XP_016876706.1:p.Thr83Ser
NM_001099274.3:c.890C>G MANE Select	NP_001092744.1:p.Thr297Ser
NM_001363668.2:c.785C>G	NP_001350597.1:p.Thr262Ser