Canonical Allele Identifier: CA407441041
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154781C>T , CM000681.2:g.55154781C>T GRCh38
NC_000019.9:g.55666149C>T , CM000681.1:g.55666149C>T GRCh37
NC_000019.8:g.60357961C>T NCBI36
NG_007866.2:g.7952G>A , LRG_432:g.7952G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.332G>A MANE Select ENSP00000341838.5:p.Arg111Lys
ENST00000665070.1:c.332G>A ENSP00000499482.1:p.Arg111Lys
ENST00000344887.9:c.332G>A ENSP00000341838.5:p.Arg111Lys
ENST00000585806.5:n.331G>A
ENST00000586669.5:n.340G>A
ENST00000587176.5:n.516G>A
ENST00000587871.1:c.951G>A
ENST00000588882.1:c.257G>A ENSP00000466729.1:p.Arg86Lys
ENST00000590463.1:n.504G>A
NM_000363.4:c.332G>A , LRG_432t1:c.332G>A NP_000354.4:p.Arg111Lys
NM_000363.5:c.332G>A MANE Select NP_000354.4:p.Arg111Lys