Canonical Allele Identifier: CA389225452

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709833C>T (hg19) ; chr14:g.24240627C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240627C>T , CM000676.2:g.24240627C>T	GRCh38
NC_000014.8:g.24709833C>T , CM000676.1:g.24709833C>T	GRCh37
NC_000014.7:g.23779673C>T	NCBI36
NG_016650.1:g.7048G>A
NG_054634.1:g.13211C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1156G>A
ENST00000557921.3:c.745G>A	ENSP00000453157.3:p.Val249Ile
ENST00000699682.1:n.1243G>A
ENST00000699683.1:n.1293G>A
ENST00000699684.1:c.*446G>A	ENSP00000514523.1:n.*446G>A
ENST00000699685.1:n.1057G>A
ENST00000699686.1:c.646G>A	ENSP00000514524.1:p.Val216Ile
ENST00000699687.1:c.748G>A	ENSP00000514525.1:p.Val250Ile
ENST00000699688.1:n.1053G>A
ENST00000699689.1:n.1409G>A
ENST00000699690.1:n.1606G>A
ENST00000699691.1:n.1750G>A
ENST00000699693.1:n.1270G>A
ENST00000699694.1:n.1512G>A
ENST00000699695.1:c.*225G>A	ENSP00000514526.1:n.*225G>A
ENST00000699696.1:n.1156G>A
ENST00000699697.1:c.853G>A	ENSP00000514527.1:p.Val285Ile
ENST00000699698.1:n.774G>A
ENST00000699699.1:n.1177G>A
ENST00000699700.1:n.1300G>A
ENST00000699701.1:c.*233G>A	ENSP00000514528.1:n.*233G>A
ENST00000267415.12:c.853G>A MANE Select	ENSP00000267415.7:p.Val285Ile
ENST00000557921.2:c.745G>A	ENSP00000453157.2:p.Val249Ile
ENST00000646753.1:c.748G>A	ENSP00000494065.1:p.Val250Ile
ENST00000267415.11:c.853G>A	ENSP00000267415.7:p.Val285Ile
ENST00000399423.8:c.853G>A	ENSP00000382350.4:p.Val285Ile
ENST00000558476.5:c.415G>A	ENSP00000452724.1:p.Val139Ile
ENST00000558566.1:c.*225G>A	ENSP00000453025.1:n.*225G>A
ENST00000559019.1:c.*225G>A	ENSP00000453675.1:n.*225G>A
ENST00000559549.1:n.579G>A
ENST00000559969.5:c.757+52G>A
ENST00000626689.2:c.*225G>A	ENSP00000486681.1:n.*225G>A
NM_001099274.1:c.853G>A	NP_001092744.1:p.Val285Ile
NM_012461.2:c.853G>A	NP_036593.2:p.Val285Ile
XM_005267528.2:c.853G>A	XP_005267585.1:p.Val285Ile
XM_005267529.2:c.748G>A	XP_005267586.1:p.Val250Ile
NM_001099274.2:c.853G>A	NP_001092744.1:p.Val285Ile
NM_001363668.1:c.748G>A	NP_001350597.1:p.Val250Ile
NM_012461.3:c.853G>A	NP_036593.2:p.Val285Ile
XM_011536642.2:c.*233G>A	XP_011534944.1:n.*233G>A
XM_017021216.2:c.211G>A	XP_016876705.1:p.Val71Ile
XM_017021217.1:c.211G>A	XP_016876706.1:p.Val71Ile
NM_001099274.3:c.853G>A MANE Select	NP_001092744.1:p.Val285Ile
NM_001363668.2:c.748G>A	NP_001350597.1:p.Val250Ile