Canonical Allele Identifier: CA2343275079
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156132A= , CM000681.2:g.55156132A= GRCh38
NC_000019.9:g.55667500A= , CM000681.1:g.55667500A= GRCh37
NC_000019.8:g.60359312A= NCBI36
NG_007866.2:g.6601T= , LRG_432:g.6601T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.282+69T= MANE Select ENSP00000341838.5:n.282+69T=
ENST00000665070.1:c.282+69T= ENSP00000499482.1:n.282+69T=
ENST00000344887.9:c.282+69T= ENSP00000341838.5:n.282+69T=
ENST00000585806.5:n.281+69T=
ENST00000586669.5:n.290+69T=
ENST00000587176.5:n.466+69T=
ENST00000587871.1:c.901+69T=
ENST00000588882.1:c.207+69T= ENSP00000466729.1:n.207+69T=
ENST00000590463.1:n.454+69T=
NM_000363.4:c.282+69T= , LRG_432t1:c.282+69T= NP_000354.4:n.282+69T=
NM_000363.5:c.282+69T= MANE Select NP_000354.4:n.282+69T=