Canonical Allele Identifier: CA2343273602
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153805C= , CM000681.2:g.55153805C= GRCh38
NC_000019.9:g.55665173C= , CM000681.1:g.55665173C= GRCh37
NC_000019.8:g.60356985C= NCBI36
NG_007866.2:g.8928G= , LRG_432:g.8928G=
NG_011829.2:g.434G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+225G= MANE Select ENSP00000341838.5:n.549+225G=
ENST00000665070.1:c.582+225G= ENSP00000499482.1:n.582+225G=
ENST00000344887.9:c.549+225G= ENSP00000341838.5:n.549+225G=
ENST00000585806.5:n.548+225G=
ENST00000588882.1:c.474+225G= ENSP00000466729.1:n.474+225G=
ENST00000589864.1:n.377+225G=
NM_000363.4:c.549+225G= , LRG_432t1:c.549+225G= NP_000354.4:n.549+225G=
NM_000363.5:c.549+225G= MANE Select NP_000354.4:n.549+225G=
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