Canonical Allele Identifier: CA407439356
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151834T>G , CM000681.2:g.55151834T>G GRCh38
NC_000019.9:g.55663202T>G , CM000681.1:g.55663202T>G GRCh37
NC_000019.8:g.60355014T>G NCBI36
NG_007866.2:g.10899A>C , LRG_432:g.10899A>C
NG_011829.2:g.2405A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.633A>C MANE Select ENSP00000341838.5:p.Ter211Cys
ENST00000665070.1:c.666A>C ENSP00000499482.1:p.Ter222Cys
ENST00000344887.9:c.633A>C ENSP00000341838.5:p.Ter211Cys
ENST00000585806.5:n.632A>C
ENST00000588882.1:c.558A>C ENSP00000466729.1:p.Ter186Cys
ENST00000589864.1:n.461A>C
NM_000363.4:c.633A>C , LRG_432t1:c.633A>C NP_000354.4:p.Ter211Cys
NM_000363.5:c.633A>C MANE Select NP_000354.4:p.Ter211Cys