Canonical Allele Identifier: CA2343273856
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154282T= , CM000681.2:g.55154282T= GRCh38
NC_000019.9:g.55665650T= , CM000681.1:g.55665650T= GRCh37
NC_000019.8:g.60357462T= NCBI36
NG_007866.2:g.8451A= , LRG_432:g.8451A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.373-76A= MANE Select ENSP00000341838.5:n.373-76A=
ENST00000665070.1:c.406-76A= ENSP00000499482.1:n.406-76A=
ENST00000344887.9:c.373-76A= ENSP00000341838.5:n.373-76A=
ENST00000585806.5:n.372-76A=
ENST00000586669.5:n.381-76A=
ENST00000588882.1:c.298-76A= ENSP00000466729.1:n.298-76A=
ENST00000589864.1:n.125A=
NM_000363.4:c.373-76A= , LRG_432t1:c.373-76A= NP_000354.4:n.373-76A=
NM_000363.5:c.373-76A= MANE Select NP_000354.4:n.373-76A=