Canonical Allele Identifier: CA389223644

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709667A>C (hg19) ; chr14:g.24240461A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240461A>C , CM000676.2:g.24240461A>C	GRCh38
NC_000014.8:g.24709667A>C , CM000676.1:g.24709667A>C	GRCh37
NC_000014.7:g.23779507A>C	NCBI36
NG_016650.1:g.7214T>G
NG_054634.1:g.13045A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1322T>G
ENST00000557921.3:c.911T>G	ENSP00000453157.3:p.Leu304Arg
ENST00000699682.1:n.1409T>G
ENST00000699683.1:n.1459T>G
ENST00000699684.1:c.*612T>G	ENSP00000514523.1:n.*612T>G
ENST00000699685.1:n.1223T>G
ENST00000699686.1:c.812T>G	ENSP00000514524.1:p.Leu271Arg
ENST00000699687.1:c.914T>G	ENSP00000514525.1:p.Leu305Arg
ENST00000699688.1:n.1219T>G
ENST00000699689.1:n.1575T>G
ENST00000699690.1:n.1772T>G
ENST00000699691.1:n.1916T>G
ENST00000699693.1:n.1436T>G
ENST00000699694.1:n.1678T>G
ENST00000699695.1:c.*391T>G	ENSP00000514526.1:n.*391T>G
ENST00000699696.1:n.1322T>G
ENST00000699697.1:c.1019T>G	ENSP00000514527.1:p.Leu340Arg
ENST00000699698.1:n.940T>G
ENST00000699699.1:n.1343T>G
ENST00000699700.1:n.1466T>G
ENST00000699701.1:c.*399T>G	ENSP00000514528.1:n.*399T>G
ENST00000267415.12:c.1019T>G MANE Select	ENSP00000267415.7:p.Leu340Arg
ENST00000646753.1:c.914T>G	ENSP00000494065.1:p.Leu305Arg
ENST00000267415.11:c.1019T>G	ENSP00000267415.7:p.Leu340Arg
ENST00000399423.8:c.1019T>G	ENSP00000382350.4:p.Leu340Arg
ENST00000557915.1:n.138T>G
ENST00000558566.1:c.*391T>G	ENSP00000453025.1:n.*391T>G
ENST00000559969.5:c.777T>G
ENST00000560019.5:c.14T>G	ENSP00000453113.1:p.Leu5Arg
ENST00000626689.2:c.*391T>G	ENSP00000486681.1:n.*391T>G
NM_001099274.1:c.1019T>G	NP_001092744.1:p.Leu340Arg
NM_012461.2:c.1019T>G	NP_036593.2:p.Leu340Arg
XM_005267528.2:c.1019T>G	XP_005267585.1:p.Leu340Arg
XM_005267529.2:c.914T>G	XP_005267586.1:p.Leu305Arg
NM_001099274.2:c.1019T>G	NP_001092744.1:p.Leu340Arg
NM_001363668.1:c.914T>G	NP_001350597.1:p.Leu305Arg
NM_012461.3:c.1019T>G	NP_036593.2:p.Leu340Arg
XM_011536642.2:c.*399T>G	XP_011534944.1:n.*399T>G
XM_017021216.2:c.377T>G	XP_016876705.1:p.Leu126Arg
XM_017021217.1:c.377T>G	XP_016876706.1:p.Leu126Arg
NM_001099274.3:c.1019T>G MANE Select	NP_001092744.1:p.Leu340Arg
NM_001363668.2:c.914T>G	NP_001350597.1:p.Leu305Arg