Canonical Allele Identifier: CA2343273742
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154083A= , CM000681.2:g.55154083A= GRCh38
NC_000019.9:g.55665451A= , CM000681.1:g.55665451A= GRCh37
NC_000019.8:g.60357263A= NCBI36
NG_007866.2:g.8650T= , LRG_432:g.8650T=
NG_011829.2:g.156T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.496T= MANE Select ENSP00000341838.5:p.Ser166=
ENST00000665070.1:c.529T= ENSP00000499482.1:p.Ser177=
ENST00000344887.9:c.496T= ENSP00000341838.5:p.Ser166=
ENST00000585806.5:n.495T=
ENST00000588882.1:c.421T= ENSP00000466729.1:p.Ser141=
ENST00000589864.1:n.324T=
NM_000363.4:c.496T= , LRG_432t1:c.496T= NP_000354.4:p.Ser166=
NM_000363.5:c.496T= MANE Select NP_000354.4:p.Ser166=