Canonical Allele Identifier: CA2343273664
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153958C= , CM000681.2:g.55153958C= GRCh38
NC_000019.9:g.55665326C= , CM000681.1:g.55665326C= GRCh37
NC_000019.8:g.60357138C= NCBI36
NG_007866.2:g.8775G= , LRG_432:g.8775G=
NG_011829.2:g.281G=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+72G= MANE Select ENSP00000341838.5:n.549+72G=
ENST00000665070.1:c.582+72G= ENSP00000499482.1:n.582+72G=
ENST00000344887.9:c.549+72G= ENSP00000341838.5:n.549+72G=
ENST00000585806.5:n.548+72G=
ENST00000588882.1:c.474+72G= ENSP00000466729.1:n.474+72G=
ENST00000589864.1:n.377+72G=
NM_000363.4:c.549+72G= , LRG_432t1:c.549+72G= NP_000354.4:n.549+72G=
NM_000363.5:c.549+72G= MANE Select NP_000354.4:n.549+72G=