Canonical Allele Identifier: CA2343273651
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153921G= , CM000681.2:g.55153921G= GRCh38
NC_000019.9:g.55665289G= , CM000681.1:g.55665289G= GRCh37
NC_000019.8:g.60357101G= NCBI36
NG_007866.2:g.8812C= , LRG_432:g.8812C=
NG_011829.2:g.318C=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+109C= MANE Select ENSP00000341838.5:n.549+109C=
ENST00000665070.1:c.582+109C= ENSP00000499482.1:n.582+109C=
ENST00000344887.9:c.549+109C= ENSP00000341838.5:n.549+109C=
ENST00000585806.5:n.548+109C=
ENST00000588882.1:c.474+109C= ENSP00000466729.1:n.474+109C=
ENST00000589864.1:n.377+109C=
NM_000363.4:c.549+109C= , LRG_432t1:c.549+109C= NP_000354.4:n.549+109C=
NM_000363.5:c.549+109C= MANE Select NP_000354.4:n.549+109C=
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