Canonical Allele Identifier: CA2343275092
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156165C= , CM000681.2:g.55156165C= GRCh38
NC_000019.9:g.55667533C= , CM000681.1:g.55667533C= GRCh37
NC_000019.8:g.60359345C= NCBI36
NG_007866.2:g.6568G= , LRG_432:g.6568G=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.282+36G= MANE Select ENSP00000341838.5:n.282+36G=
ENST00000665070.1:c.282+36G= ENSP00000499482.1:n.282+36G=
ENST00000344887.9:c.282+36G= ENSP00000341838.5:n.282+36G=
ENST00000585806.5:n.281+36G=
ENST00000586669.5:n.290+36G=
ENST00000587176.5:n.466+36G=
ENST00000587871.1:c.901+36G=
ENST00000588882.1:c.207+36G= ENSP00000466729.1:n.207+36G=
ENST00000590463.1:n.454+36G=
NM_000363.4:c.282+36G= , LRG_432t1:c.282+36G= NP_000354.4:n.282+36G=
NM_000363.5:c.282+36G= MANE Select NP_000354.4:n.282+36G=