Canonical Allele Identifier: CA2343273962
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154526C= , CM000681.2:g.55154526C= GRCh38
NC_000019.9:g.55665894C= , CM000681.1:g.55665894C= GRCh37
NC_000019.8:g.60357706C= NCBI36
NG_007866.2:g.8207G= , LRG_432:g.8207G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.372+215G= MANE Select ENSP00000341838.5:n.372+215G=
ENST00000665070.1:c.405+182G= ENSP00000499482.1:n.405+182G=
ENST00000344887.9:c.372+215G= ENSP00000341838.5:n.372+215G=
ENST00000585806.5:n.371+215G=
ENST00000586669.5:n.380+215G=
ENST00000587176.5:n.771G=
ENST00000588882.1:c.297+215G= ENSP00000466729.1:n.297+215G=
NM_000363.4:c.372+215G= , LRG_432t1:c.372+215G= NP_000354.4:n.372+215G=
NM_000363.5:c.372+215G= MANE Select NP_000354.4:n.372+215G=
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