Canonical Allele Identifier: CA2343273766
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154123A= , CM000681.2:g.55154123A= GRCh38
NC_000019.9:g.55665491A= , CM000681.1:g.55665491A= GRCh37
NC_000019.8:g.60357303A= NCBI36
NG_007866.2:g.8610T= , LRG_432:g.8610T=
NG_011829.2:g.116T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.456T= MANE Select ENSP00000341838.5:p.Asp152=
ENST00000665070.1:c.489T= ENSP00000499482.1:p.Asp163=
ENST00000344887.9:c.456T= ENSP00000341838.5:p.Asp152=
ENST00000585806.5:n.455T=
ENST00000586669.5:n.464T=
ENST00000588882.1:c.381T= ENSP00000466729.1:p.Asp127=
ENST00000589864.1:n.284T=
NM_000363.4:c.456T= , LRG_432t1:c.456T= NP_000354.4:p.Asp152=
NM_000363.5:c.456T= MANE Select NP_000354.4:p.Asp152=