Canonical Allele Identifier: CA2814881294
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153814T>A , CM000681.2:g.55153814T>A GRCh38
NC_000019.9:g.55665182T>A , CM000681.1:g.55665182T>A GRCh37
NC_000019.8:g.60356994T>A NCBI36
NG_007866.2:g.8919A>T , LRG_432:g.8919A>T
NG_011829.2:g.425A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+216A>T MANE Select ENSP00000341838.5:n.549+216A>T
ENST00000665070.1:c.582+216A>T ENSP00000499482.1:n.582+216A>T
ENST00000344887.9:c.549+216A>T ENSP00000341838.5:n.549+216A>T
ENST00000585806.5:n.548+216A>T
ENST00000588882.1:c.474+216A>T ENSP00000466729.1:n.474+216A>T
ENST00000589864.1:n.377+216A>T
NM_000363.4:c.549+216A>T , LRG_432t1:c.549+216A>T NP_000354.4:n.549+216A>T
NM_000363.5:c.549+216A>T MANE Select NP_000354.4:n.549+216A>T
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