Canonical Allele Identifier: CA2343275093
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156166G= , CM000681.2:g.55156166G= GRCh38
NC_000019.9:g.55667534G= , CM000681.1:g.55667534G= GRCh37
NC_000019.8:g.60359346G= NCBI36
NG_007866.2:g.6567C= , LRG_432:g.6567C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.282+35C= MANE Select ENSP00000341838.5:n.282+35C=
ENST00000665070.1:c.282+35C= ENSP00000499482.1:n.282+35C=
ENST00000344887.9:c.282+35C= ENSP00000341838.5:n.282+35C=
ENST00000585806.5:n.281+35C=
ENST00000586669.5:n.290+35C=
ENST00000587176.5:n.466+35C=
ENST00000587871.1:c.901+35C=
ENST00000588882.1:c.207+35C= ENSP00000466729.1:n.207+35C=
ENST00000590463.1:n.454+35C=
NM_000363.4:c.282+35C= , LRG_432t1:c.282+35C= NP_000354.4:n.282+35C=
NM_000363.5:c.282+35C= MANE Select NP_000354.4:n.282+35C=