Canonical Allele Identifier: CA2343273700
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154026T= , CM000681.2:g.55154026T= GRCh38
NC_000019.9:g.55665394T= , CM000681.1:g.55665394T= GRCh37
NC_000019.8:g.60357206T= NCBI36
NG_007866.2:g.8707A= , LRG_432:g.8707A=
NG_011829.2:g.213A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+4A= MANE Select ENSP00000341838.5:n.549+4A=
ENST00000665070.1:c.582+4A= ENSP00000499482.1:n.582+4A=
ENST00000344887.9:c.549+4A= ENSP00000341838.5:n.549+4A=
ENST00000585806.5:n.548+4A=
ENST00000588882.1:c.474+4A= ENSP00000466729.1:n.474+4A=
ENST00000589864.1:n.377+4A=
NM_000363.4:c.549+4A= , LRG_432t1:c.549+4A= NP_000354.4:n.549+4A=
NM_000363.5:c.549+4A= MANE Select NP_000354.4:n.549+4A=