Canonical Allele Identifier: CA2343273762
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154115A= , CM000681.2:g.55154115A= GRCh38
NC_000019.9:g.55665483A= , CM000681.1:g.55665483A= GRCh37
NC_000019.8:g.60357295A= NCBI36
NG_007866.2:g.8618T= , LRG_432:g.8618T=
NG_011829.2:g.124T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.464T= MANE Select ENSP00000341838.5:p.Met155=
ENST00000665070.1:c.497T= ENSP00000499482.1:p.Met166=
ENST00000344887.9:c.464T= ENSP00000341838.5:p.Met155=
ENST00000585806.5:n.463T=
ENST00000586669.5:n.472T=
ENST00000588882.1:c.389T= ENSP00000466729.1:p.Met130=
ENST00000589864.1:n.292T=
NM_000363.4:c.464T= , LRG_432t1:c.464T= NP_000354.4:p.Met155=
NM_000363.5:c.464T= MANE Select NP_000354.4:p.Met155=