Canonical Allele Identifier: CA2343273691
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2085710730
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154009del , CM000681.2:g.55154009del GRCh38
NC_000019.9:g.55665377del , CM000681.1:g.55665377del GRCh37
NC_000019.8:g.60357189del NCBI36
NG_007866.2:g.8725del , LRG_432:g.8725del
NG_011829.2:g.231del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+22del MANE Select ENSP00000341838.5:n.549+22del
ENST00000665070.1:c.582+22del ENSP00000499482.1:n.582+22del
ENST00000344887.9:c.549+22del ENSP00000341838.5:n.549+22del
ENST00000585806.5:n.548+22del
ENST00000588882.1:c.474+22del ENSP00000466729.1:n.474+22del
ENST00000589864.1:n.377+22del
NM_000363.4:c.549+22del , LRG_432t1:c.549+22del NP_000354.4:n.549+22del
NM_000363.5:c.549+22del MANE Select NP_000354.4:n.549+22del
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