Canonical Allele Identifier: CA2343274149
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154867C= , CM000681.2:g.55154867C= GRCh38
NC_000019.9:g.55666235C= , CM000681.1:g.55666235C= GRCh37
NC_000019.8:g.60358047C= NCBI36
NG_007866.2:g.7866G= , LRG_432:g.7866G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.283-37G= MANE Select ENSP00000341838.5:n.283-37G=
ENST00000665070.1:c.283-37G= ENSP00000499482.1:n.283-37G=
ENST00000344887.9:c.283-37G= ENSP00000341838.5:n.283-37G=
ENST00000585806.5:n.282-37G=
ENST00000586669.5:n.291-37G=
ENST00000587176.5:n.467-37G=
ENST00000587871.1:c.902-37G=
ENST00000588882.1:c.208-37G= ENSP00000466729.1:n.208-37G=
ENST00000590463.1:n.455-37G=
NM_000363.4:c.283-37G= , LRG_432t1:c.283-37G= NP_000354.4:n.283-37G=
NM_000363.5:c.283-37G= MANE Select NP_000354.4:n.283-37G=
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