Canonical Allele Identifier: CA407440391
Gene: TNNI3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55665474A>T (hg19) chr19:g.55154106A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154106A>T , CM000681.2:g.55154106A>T GRCh38
NC_000019.9:g.55665474A>T , CM000681.1:g.55665474A>T GRCh37
NC_000019.8:g.60357286A>T NCBI36
NG_007866.2:g.8627T>A , LRG_432:g.8627T>A
NG_011829.2:g.133T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.473T>A MANE Select ENSP00000341838.5:p.Leu158Gln
ENST00000665070.1:c.506T>A ENSP00000499482.1:p.Leu169Gln
ENST00000344887.9:c.473T>A ENSP00000341838.5:p.Leu158Gln
ENST00000585806.5:n.472T>A
ENST00000588882.1:c.398T>A ENSP00000466729.1:p.Leu133Gln
ENST00000589864.1:n.301T>A
NM_000363.4:c.473T>A , LRG_432t1:c.473T>A NP_000354.4:p.Leu158Gln
NM_000363.5:c.473T>A MANE Select NP_000354.4:p.Leu158Gln
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