Canonical Allele Identifier: CA2814881300
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153852C>T , CM000681.2:g.55153852C>T GRCh38
NC_000019.9:g.55665220C>T , CM000681.1:g.55665220C>T GRCh37
NC_000019.8:g.60357032C>T NCBI36
NG_007866.2:g.8881G>A , LRG_432:g.8881G>A
NG_011829.2:g.387G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+178G>A MANE Select ENSP00000341838.5:n.549+178G>A
ENST00000665070.1:c.582+178G>A ENSP00000499482.1:n.582+178G>A
ENST00000344887.9:c.549+178G>A ENSP00000341838.5:n.549+178G>A
ENST00000585806.5:n.548+178G>A
ENST00000588882.1:c.474+178G>A ENSP00000466729.1:n.474+178G>A
ENST00000589864.1:n.377+178G>A
NM_000363.4:c.549+178G>A , LRG_432t1:c.549+178G>A NP_000354.4:n.549+178G>A
NM_000363.5:c.549+178G>A MANE Select NP_000354.4:n.549+178G>A
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