Canonical Allele Identifier: CA2343274028
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154669G= , CM000681.2:g.55154669G= GRCh38
NC_000019.9:g.55666037G= , CM000681.1:g.55666037G= GRCh37
NC_000019.8:g.60357849G= NCBI36
NG_007866.2:g.8064C= , LRG_432:g.8064C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.372+72C= MANE Select ENSP00000341838.5:n.372+72C=
ENST00000665070.1:c.405+39C= ENSP00000499482.1:n.405+39C=
ENST00000344887.9:c.372+72C= ENSP00000341838.5:n.372+72C=
ENST00000585806.5:n.371+72C=
ENST00000586669.5:n.380+72C=
ENST00000587176.5:n.628C=
ENST00000588882.1:c.297+72C= ENSP00000466729.1:n.297+72C=
NM_000363.4:c.372+72C= , LRG_432t1:c.372+72C= NP_000354.4:n.372+72C=
NM_000363.5:c.372+72C= MANE Select NP_000354.4:n.372+72C=