Canonical Allele Identifier: CA2343275080
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156137A= , CM000681.2:g.55156137A= GRCh38
NC_000019.9:g.55667505A= , CM000681.1:g.55667505A= GRCh37
NC_000019.8:g.60359317A= NCBI36
NG_007866.2:g.6596T= , LRG_432:g.6596T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.282+64T= MANE Select ENSP00000341838.5:n.282+64T=
ENST00000665070.1:c.282+64T= ENSP00000499482.1:n.282+64T=
ENST00000344887.9:c.282+64T= ENSP00000341838.5:n.282+64T=
ENST00000585806.5:n.281+64T=
ENST00000586669.5:n.290+64T=
ENST00000587176.5:n.466+64T=
ENST00000587871.1:c.901+64T=
ENST00000588882.1:c.207+64T= ENSP00000466729.1:n.207+64T=
ENST00000590463.1:n.454+64T=
NM_000363.4:c.282+64T= , LRG_432t1:c.282+64T= NP_000354.4:n.282+64T=
NM_000363.5:c.282+64T= MANE Select NP_000354.4:n.282+64T=