Canonical Allele Identifier: CA2343273798
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154181A= , CM000681.2:g.55154181A= GRCh38
NC_000019.9:g.55665549A= , CM000681.1:g.55665549A= GRCh37
NC_000019.8:g.60357361A= NCBI36
NG_007866.2:g.8552T= , LRG_432:g.8552T=
NG_011829.2:g.58T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.398T= MANE Select ENSP00000341838.5:p.Phe133=
ENST00000665070.1:c.431T= ENSP00000499482.1:p.Phe144=
ENST00000344887.9:c.398T= ENSP00000341838.5:p.Phe133=
ENST00000585806.5:n.397T=
ENST00000586669.5:n.406T=
ENST00000588882.1:c.323T= ENSP00000466729.1:p.Phe108=
ENST00000589864.1:n.226T=
NM_000363.4:c.398T= , LRG_432t1:c.398T= NP_000354.4:p.Phe133=
NM_000363.5:c.398T= MANE Select NP_000354.4:p.Phe133=