Canonical Allele Identifier: CA389224814
Gene: TINF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240564T>C , CM000676.2:g.24240564T>C GRCh38
NC_000014.8:g.24709770T>C , CM000676.1:g.24709770T>C GRCh37
NC_000014.7:g.23779610T>C NCBI36
NG_016650.1:g.7111A>G
NG_054634.1:g.13148T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1219A>G
ENST00000557921.3:c.808A>G ENSP00000453157.3:p.Lys270Glu
ENST00000699682.1:n.1306A>G
ENST00000699683.1:n.1356A>G
ENST00000699684.1:c.*509A>G ENSP00000514523.1:n.*509A>G
ENST00000699685.1:n.1120A>G
ENST00000699686.1:c.709A>G ENSP00000514524.1:p.Lys237Glu
ENST00000699687.1:c.811A>G ENSP00000514525.1:p.Lys271Glu
ENST00000699688.1:n.1116A>G
ENST00000699689.1:n.1472A>G
ENST00000699690.1:n.1669A>G
ENST00000699691.1:n.1813A>G
ENST00000699693.1:n.1333A>G
ENST00000699694.1:n.1575A>G
ENST00000699695.1:c.*288A>G ENSP00000514526.1:n.*288A>G
ENST00000699696.1:n.1219A>G
ENST00000699697.1:c.916A>G ENSP00000514527.1:p.Lys306Glu
ENST00000699698.1:n.837A>G
ENST00000699699.1:n.1240A>G
ENST00000699700.1:n.1363A>G
ENST00000699701.1:c.*296A>G ENSP00000514528.1:n.*296A>G
ENST00000267415.12:c.916A>G MANE Select ENSP00000267415.7:p.Lys306Glu
ENST00000557921.2:c.808A>G ENSP00000453157.2:p.Lys270Glu
ENST00000646753.1:c.811A>G ENSP00000494065.1:p.Lys271Glu
ENST00000267415.11:c.916A>G ENSP00000267415.7:p.Lys306Glu
ENST00000399423.8:c.916A>G ENSP00000382350.4:p.Lys306Glu
ENST00000557915.1:n.35A>G
ENST00000558566.1:c.*288A>G ENSP00000453025.1:n.*288A>G
ENST00000559019.1:c.*288A>G ENSP00000453675.1:n.*288A>G
ENST00000559969.5:c.758-84A>G
ENST00000626689.2:c.*288A>G ENSP00000486681.1:n.*288A>G
NM_001099274.1:c.916A>G NP_001092744.1:p.Lys306Glu
NM_012461.2:c.916A>G NP_036593.2:p.Lys306Glu
XM_005267528.2:c.916A>G XP_005267585.1:p.Lys306Glu
XM_005267529.2:c.811A>G XP_005267586.1:p.Lys271Glu
NM_001099274.2:c.916A>G NP_001092744.1:p.Lys306Glu
NM_001363668.1:c.811A>G NP_001350597.1:p.Lys271Glu
NM_012461.3:c.916A>G NP_036593.2:p.Lys306Glu
XM_011536642.2:c.*296A>G XP_011534944.1:n.*296A>G
XM_017021216.2:c.274A>G XP_016876705.1:p.Lys92Glu
XM_017021217.1:c.274A>G XP_016876706.1:p.Lys92Glu
NM_001099274.3:c.916A>G MANE Select NP_001092744.1:p.Lys306Glu
NM_001363668.2:c.811A>G NP_001350597.1:p.Lys271Glu