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Canonical Allele Identifier: Get Identifier
Gene: TINF2 HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
ENSP00000452724.1:p.Thr138Pro
ENST00000558476.5:c.[412A>C;417C>A]

ENST00000558476.5:c.[412A>C;417C=]

ENST00000558476.5:c.[412A>C;417C>G]

ENST00000558476.5:c.[412A>C;417C>T]

ENST00000558476.5:c.[412A>C;418A=]

ENST00000558476.5:c.[412A>C;421C>T]

ENST00000558476.5:c.[412A>C;422T=]

ENST00000558476.5:c.[412A>C;423G>A]

ENST00000558476.5:c.[412A>C;423G>C]

ENST00000558476.5:c.[412A>C;423G=]

ENST00000558476.5:c.[412A>C;423G>T]

ENST00000558476.5:c.[412A>C;424T=]

ENST00000558476.5:c.[412A>C;426T>C]

ENST00000558476.5:c.[412A>C;427C=]

ENST00000558476.5:c.[412A>C;427_428delins...

ENST00000558476.5:c.[412A>C;429C>A]

ENST00000558476.5:c.[412A>C;429C=]

ENST00000558476.5:c.[412A>C;429C>G]

ENST00000558476.5:c.[412A>C;429C>T]

ENST00000558476.5:c.[412A>C;432T>C]

ENST00000558476.5:c.[412A>C;433A=]

ENST00000558476.5:c.[412A>C;433A>C]

ENST00000558476.5:c.[412A>C;435G>A]