Canonical Allele Identifier: CA389223633
Gene: TINF2 HGNC NCBI

Linked Data

dbSNP Id: rs2040547924

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240458T>C , CM000676.2:g.24240458T>C GRCh38
NC_000014.8:g.24709664T>C , CM000676.1:g.24709664T>C GRCh37
NC_000014.7:g.23779504T>C NCBI36
NG_016650.1:g.7217A>G
NG_054634.1:g.13042T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1325A>G
ENST00000557921.3:c.914A>G ENSP00000453157.3:p.Lys305Arg
ENST00000699682.1:n.1412A>G
ENST00000699683.1:n.1462A>G
ENST00000699684.1:c.*615A>G ENSP00000514523.1:n.*615A>G
ENST00000699685.1:n.1226A>G
ENST00000699686.1:c.815A>G ENSP00000514524.1:p.Lys272Arg
ENST00000699687.1:c.917A>G ENSP00000514525.1:p.Lys306Arg
ENST00000699688.1:n.1222A>G
ENST00000699689.1:n.1578A>G
ENST00000699690.1:n.1775A>G
ENST00000699691.1:n.1919A>G
ENST00000699693.1:n.1439A>G
ENST00000699694.1:n.1681A>G
ENST00000699695.1:c.*394A>G ENSP00000514526.1:n.*394A>G
ENST00000699696.1:n.1325A>G
ENST00000699697.1:c.1022A>G ENSP00000514527.1:p.Lys341Arg
ENST00000699698.1:n.943A>G
ENST00000699699.1:n.1346A>G
ENST00000699700.1:n.1469A>G
ENST00000699701.1:c.*402A>G ENSP00000514528.1:n.*402A>G
ENST00000267415.12:c.1022A>G MANE Select ENSP00000267415.7:p.Lys341Arg
ENST00000646753.1:c.917A>G ENSP00000494065.1:p.Lys306Arg
ENST00000267415.11:c.1022A>G ENSP00000267415.7:p.Lys341Arg
ENST00000399423.8:c.1022A>G ENSP00000382350.4:p.Lys341Arg
ENST00000557915.1:n.141A>G
ENST00000558566.1:c.*394A>G ENSP00000453025.1:n.*394A>G
ENST00000559969.5:c.780A>G
ENST00000560019.5:c.17A>G ENSP00000453113.1:p.Lys6Arg
ENST00000626689.2:c.*394A>G ENSP00000486681.1:n.*394A>G
NM_001099274.1:c.1022A>G NP_001092744.1:p.Lys341Arg
NM_012461.2:c.1022A>G NP_036593.2:p.Lys341Arg
XM_005267528.2:c.1022A>G XP_005267585.1:p.Lys341Arg
XM_005267529.2:c.917A>G XP_005267586.1:p.Lys306Arg
NM_001099274.2:c.1022A>G NP_001092744.1:p.Lys341Arg
NM_001363668.1:c.917A>G NP_001350597.1:p.Lys306Arg
NM_012461.3:c.1022A>G NP_036593.2:p.Lys341Arg
XM_011536642.2:c.*402A>G XP_011534944.1:n.*402A>G
XM_017021216.2:c.380A>G XP_016876705.1:p.Lys127Arg
XM_017021217.1:c.380A>G XP_016876706.1:p.Lys127Arg
NM_001099274.3:c.1022A>G MANE Select NP_001092744.1:p.Lys341Arg
NM_001363668.2:c.917A>G NP_001350597.1:p.Lys306Arg