Canonical Allele Identifier: CA2343274139
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154844G= , CM000681.2:g.55154844G= GRCh38
NC_000019.9:g.55666212G= , CM000681.1:g.55666212G= GRCh37
NC_000019.8:g.60358024G= NCBI36
NG_007866.2:g.7889C= , LRG_432:g.7889C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.283-14C= MANE Select ENSP00000341838.5:n.283-14C=
ENST00000665070.1:c.283-14C= ENSP00000499482.1:n.283-14C=
ENST00000344887.9:c.283-14C= ENSP00000341838.5:n.283-14C=
ENST00000585806.5:n.282-14C=
ENST00000586669.5:n.291-14C=
ENST00000587176.5:n.467-14C=
ENST00000587871.1:c.902-14C=
ENST00000588882.1:c.208-14C= ENSP00000466729.1:n.208-14C=
ENST00000590463.1:n.455-14C=
NM_000363.4:c.283-14C= , LRG_432t1:c.283-14C= NP_000354.4:n.283-14C=
NM_000363.5:c.283-14C= MANE Select NP_000354.4:n.283-14C=