Canonical Allele Identifier: CA389222999

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709525T>C (hg19) ; chr14:g.24240319T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240319T>C , CM000676.2:g.24240319T>C	GRCh38
NC_000014.8:g.24709525T>C , CM000676.1:g.24709525T>C	GRCh37
NC_000014.7:g.23779365T>C	NCBI36
NG_016650.1:g.7356A>G
NG_054634.1:g.12903T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1464A>G
ENST00000557921.3:c.*96A>G	ENSP00000453157.3:n.*96A>G
ENST00000699682.1:n.1551A>G
ENST00000699683.1:n.1601A>G
ENST00000699684.1:c.*754A>G	ENSP00000514523.1:n.*754A>G
ENST00000699685.1:n.1365A>G
ENST00000699686.1:c.*96A>G	ENSP00000514524.1:n.*96A>G
ENST00000699687.1:c.*96A>G	ENSP00000514525.1:n.*96A>G
ENST00000699688.1:n.1361A>G
ENST00000699689.1:n.1717A>G
ENST00000699690.1:n.1914A>G
ENST00000699691.1:n.2058A>G
ENST00000699692.1:n.12A>G
ENST00000699693.1:n.1490A>G
ENST00000699694.1:n.1820A>G
ENST00000699695.1:c.*445A>G	ENSP00000514526.1:n.*445A>G
ENST00000699696.1:n.1464A>G
ENST00000699697.1:c.1073A>G	ENSP00000514527.1:p.Asp358Gly
ENST00000699698.1:n.994A>G
ENST00000699699.1:n.1485A>G
ENST00000699700.1:n.1608A>G
ENST00000699701.1:c.*541A>G	ENSP00000514528.1:n.*541A>G
ENST00000267415.12:c.1073A>G MANE Select	ENSP00000267415.7:p.Asp358Gly
ENST00000646753.1:c.968A>G	ENSP00000494065.1:p.Asp323Gly
ENST00000267415.11:c.1073A>G	ENSP00000267415.7:p.Asp358Gly
ENST00000399423.8:c.*96A>G	ENSP00000382350.4:n.*96A>G
ENST00000557915.1:n.280A>G
ENST00000558566.1:c.*533A>G	ENSP00000453025.1:n.*533A>G
ENST00000559969.5:c.919A>G
ENST00000560019.5:c.68A>G	ENSP00000453113.1:p.Asp23Gly
ENST00000626689.2:c.*445A>G	ENSP00000486681.1:n.*445A>G
NM_001099274.1:c.1073A>G	NP_001092744.1:p.Asp358Gly
NM_012461.2:c.*96A>G	NP_036593.2:n.*96A>G
XM_005267528.2:c.1073A>G	XP_005267585.1:p.Asp358Gly
XM_005267529.2:c.968A>G	XP_005267586.1:p.Asp323Gly
NM_001099274.2:c.1073A>G	NP_001092744.1:p.Asp358Gly
NM_001363668.1:c.968A>G	NP_001350597.1:p.Asp323Gly
NM_012461.3:c.*96A>G	NP_036593.2:n.*96A>G
XM_011536642.2:c.*541A>G	XP_011534944.1:n.*541A>G
XM_017021216.2:c.431A>G	XP_016876705.1:p.Asp144Gly
XM_017021217.1:c.431A>G	XP_016876706.1:p.Asp144Gly
NM_001099274.3:c.1073A>G MANE Select	NP_001092744.1:p.Asp358Gly
NM_001363668.2:c.968A>G	NP_001350597.1:p.Asp323Gly