Canonical Allele Identifier: CA2343272380
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151801C= , CM000681.2:g.55151801C= GRCh38
NC_000019.9:g.55663169C= , CM000681.1:g.55663169C= GRCh37
NC_000019.8:g.60354981C= NCBI36
NG_007866.2:g.10932G= , LRG_432:g.10932G=
NG_011829.2:g.2438G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.*33G= MANE Select ENSP00000341838.5:n.*33G=
ENST00000665070.1:c.*33G= ENSP00000499482.1:n.*33G=
ENST00000344887.9:c.*33G= ENSP00000341838.5:n.*33G=
ENST00000585806.5:n.665G=
ENST00000588882.1:c.*33G= ENSP00000466729.1:n.*33G=
ENST00000589864.1:n.494G=
NM_000363.4:c.*33G= , LRG_432t1:c.*33G= NP_000354.4:n.*33G=
NM_000363.5:c.*33G= MANE Select NP_000354.4:n.*33G=