Canonical Allele Identifier: CA407440401
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665477G>T (hg19) chr19:g.55154109G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154109G>T , CM000681.2:g.55154109G>T GRCh38
NC_000019.9:g.55665477G>T , CM000681.1:g.55665477G>T GRCh37
NC_000019.8:g.60357289G>T NCBI36
NG_007866.2:g.8624C>A , LRG_432:g.8624C>A
NG_011829.2:g.130C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.470C>A MANE Select ENSP00000341838.5:p.Ala157Glu
ENST00000665070.1:c.503C>A ENSP00000499482.1:p.Ala168Glu
ENST00000344887.9:c.470C>A ENSP00000341838.5:p.Ala157Glu
ENST00000585806.5:n.469C>A
ENST00000588882.1:c.395C>A ENSP00000466729.1:p.Ala132Glu
ENST00000589864.1:n.298C>A
NM_000363.4:c.470C>A , LRG_432t1:c.470C>A NP_000354.4:p.Ala157Glu
NM_000363.5:c.470C>A MANE Select NP_000354.4:p.Ala157Glu
Search 100 bp 5'
Search 100 bp 3'