Canonical Allele Identifier: CA2343272798
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55152174T= , CM000681.2:g.55152174T= GRCh38
NC_000019.9:g.55663542T= , CM000681.1:g.55663542T= GRCh37
NC_000019.8:g.60355354T= NCBI36
NG_007866.2:g.10559A= , LRG_432:g.10559A=
NG_011829.2:g.2065A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.550-257A= MANE Select ENSP00000341838.5:n.550-257A=
ENST00000665070.1:c.583-257A= ENSP00000499482.1:n.583-257A=
ENST00000344887.9:c.550-257A= ENSP00000341838.5:n.550-257A=
ENST00000585806.5:n.549-257A=
ENST00000588882.1:c.475-257A= ENSP00000466729.1:n.475-257A=
ENST00000589864.1:n.378-257A=
NM_000363.4:c.550-257A= , LRG_432t1:c.550-257A= NP_000354.4:n.550-257A=
NM_000363.5:c.550-257A= MANE Select NP_000354.4:n.550-257A=
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