Canonical Allele Identifier: CA2343272647
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151899C= , CM000681.2:g.55151899C= GRCh38
NC_000019.9:g.55663267C= , CM000681.1:g.55663267C= GRCh37
NC_000019.8:g.60355079C= NCBI36
NG_007866.2:g.10834G= , LRG_432:g.10834G=
NG_011829.2:g.2340G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.568G= MANE Select ENSP00000341838.5:p.Asp190=
ENST00000665070.1:c.601G= ENSP00000499482.1:p.Asp201=
ENST00000344887.9:c.568G= ENSP00000341838.5:p.Asp190=
ENST00000585806.5:n.567G=
ENST00000588882.1:c.493G= ENSP00000466729.1:p.Asp165=
ENST00000589864.1:n.396G=
NM_000363.4:c.568G= , LRG_432t1:c.568G= NP_000354.4:p.Asp190=
NM_000363.5:c.568G= MANE Select NP_000354.4:p.Asp190=