Canonical Allele Identifier: CA389225444

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709832A>C (hg19) ; chr14:g.24240626A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240626A>C , CM000676.2:g.24240626A>C	GRCh38
NC_000014.8:g.24709832A>C , CM000676.1:g.24709832A>C	GRCh37
NC_000014.7:g.23779672A>C	NCBI36
NG_016650.1:g.7049T>G
NG_054634.1:g.13210A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1157T>G
ENST00000557921.3:c.746T>G	ENSP00000453157.3:p.Val249Gly
ENST00000699682.1:n.1244T>G
ENST00000699683.1:n.1294T>G
ENST00000699684.1:c.*447T>G	ENSP00000514523.1:n.*447T>G
ENST00000699685.1:n.1058T>G
ENST00000699686.1:c.647T>G	ENSP00000514524.1:p.Val216Gly
ENST00000699687.1:c.749T>G	ENSP00000514525.1:p.Val250Gly
ENST00000699688.1:n.1054T>G
ENST00000699689.1:n.1410T>G
ENST00000699690.1:n.1607T>G
ENST00000699691.1:n.1751T>G
ENST00000699693.1:n.1271T>G
ENST00000699694.1:n.1513T>G
ENST00000699695.1:c.*226T>G	ENSP00000514526.1:n.*226T>G
ENST00000699696.1:n.1157T>G
ENST00000699697.1:c.854T>G	ENSP00000514527.1:p.Val285Gly
ENST00000699698.1:n.775T>G
ENST00000699699.1:n.1178T>G
ENST00000699700.1:n.1301T>G
ENST00000699701.1:c.*234T>G	ENSP00000514528.1:n.*234T>G
ENST00000267415.12:c.854T>G MANE Select	ENSP00000267415.7:p.Val285Gly
ENST00000557921.2:c.746T>G	ENSP00000453157.2:p.Val249Gly
ENST00000646753.1:c.749T>G	ENSP00000494065.1:p.Val250Gly
ENST00000267415.11:c.854T>G	ENSP00000267415.7:p.Val285Gly
ENST00000399423.8:c.854T>G	ENSP00000382350.4:p.Val285Gly
ENST00000558476.5:c.416T>G	ENSP00000452724.1:p.Val139Gly
ENST00000558566.1:c.*226T>G	ENSP00000453025.1:n.*226T>G
ENST00000559019.1:c.*226T>G	ENSP00000453675.1:n.*226T>G
ENST00000559549.1:n.580T>G
ENST00000559969.5:c.757+53T>G
ENST00000626689.2:c.*226T>G	ENSP00000486681.1:n.*226T>G
NM_001099274.1:c.854T>G	NP_001092744.1:p.Val285Gly
NM_012461.2:c.854T>G	NP_036593.2:p.Val285Gly
XM_005267528.2:c.854T>G	XP_005267585.1:p.Val285Gly
XM_005267529.2:c.749T>G	XP_005267586.1:p.Val250Gly
NM_001099274.2:c.854T>G	NP_001092744.1:p.Val285Gly
NM_001363668.1:c.749T>G	NP_001350597.1:p.Val250Gly
NM_012461.3:c.854T>G	NP_036593.2:p.Val285Gly
XM_011536642.2:c.*234T>G	XP_011534944.1:n.*234T>G
XM_017021216.2:c.212T>G	XP_016876705.1:p.Val71Gly
XM_017021217.1:c.212T>G	XP_016876706.1:p.Val71Gly
NM_001099274.3:c.854T>G MANE Select	NP_001092744.1:p.Val285Gly
NM_001363668.2:c.749T>G	NP_001350597.1:p.Val250Gly