Canonical Allele Identifier: CA2343272522
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151865A= , CM000681.2:g.55151865A= GRCh38
NC_000019.9:g.55663233A= , CM000681.1:g.55663233A= GRCh37
NC_000019.8:g.60355045A= NCBI36
NG_007866.2:g.10868T= , LRG_432:g.10868T=
NG_011829.2:g.2374T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.602T= MANE Select ENSP00000341838.5:p.Met201=
ENST00000665070.1:c.635T= ENSP00000499482.1:p.Met212=
ENST00000344887.9:c.602T= ENSP00000341838.5:p.Met201=
ENST00000585806.5:n.601T=
ENST00000588882.1:c.527T= ENSP00000466729.1:p.Met176=
ENST00000589864.1:n.430T=
NM_000363.4:c.602T= , LRG_432t1:c.602T= NP_000354.4:p.Met201=
NM_000363.5:c.602T= MANE Select NP_000354.4:p.Met201=