Canonical Allele Identifier: CA2587243486
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153962_55153963insTTGGCC , CM000681.2:g.55153962_55153963insTTGGCC GRCh38
NC_000019.9:g.55665330_55665331insTTGGCC , CM000681.1:g.55665330_55665331insTTGGCC GRCh37
NC_000019.8:g.60357142_60357143insTTGGCC NCBI36
NG_007866.2:g.8771_8772insGCCAAG , LRG_432:g.8771_8772insGCCAAG
NG_011829.2:g.277_278insGCCAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+68_549+69insGCCAAG MANE Select ENSP00000341838.5:n.549+68_549+69insGCCAA...
ENST00000665070.1:c.582+68_582+69insGCCAAG ENSP00000499482.1:n.582+68_582+69insGCCAA...
ENST00000344887.9:c.549+68_549+69insGCCAAG ENSP00000341838.5:n.549+68_549+69insGCCAA...
ENST00000585806.5:n.548+68_548+69insGCCAAG
ENST00000588882.1:c.474+68_474+69insGCCAAG ENSP00000466729.1:n.474+68_474+69insGCCAA...
ENST00000589864.1:n.377+68_377+69insGCCAAG
NM_000363.4:c.549+68_549+69insGCCAAG , LRG_432t1:c.549+68_549+69insGCCAAG NP_000354.4:n.549+68_549+69insGCCAAG
NM_000363.5:c.549+68_549+69insGCCAAG MANE Select NP_000354.4:n.549+68_549+69insGCCAAG