Canonical Allele Identifier: CA2343273895
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154382C= , CM000681.2:g.55154382C= GRCh38
NC_000019.9:g.55665750C= , CM000681.1:g.55665750C= GRCh37
NC_000019.8:g.60357562C= NCBI36
NG_007866.2:g.8351G= , LRG_432:g.8351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.373-176G= MANE Select ENSP00000341838.5:n.373-176G=
ENST00000665070.1:c.406-176G= ENSP00000499482.1:n.406-176G=
ENST00000344887.9:c.373-176G= ENSP00000341838.5:n.373-176G=
ENST00000585806.5:n.372-176G=
ENST00000586669.5:n.381-176G=
ENST00000587176.5:n.915G=
ENST00000588882.1:c.298-176G= ENSP00000466729.1:n.298-176G=
ENST00000589864.1:n.25G=
NM_000363.4:c.373-176G= , LRG_432t1:c.373-176G= NP_000354.4:n.373-176G=
NM_000363.5:c.373-176G= MANE Select NP_000354.4:n.373-176G=
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