Canonical Allele Identifier: CA2343273719
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154046T= , CM000681.2:g.55154046T= GRCh38
NC_000019.9:g.55665414T= , CM000681.1:g.55665414T= GRCh37
NC_000019.8:g.60357226T= NCBI36
NG_007866.2:g.8687A= , LRG_432:g.8687A=
NG_011829.2:g.193A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.533A= MANE Select ENSP00000341838.5:p.Lys178=
ENST00000665070.1:c.566A= ENSP00000499482.1:p.Lys189=
ENST00000344887.9:c.533A= ENSP00000341838.5:p.Lys178=
ENST00000585806.5:n.532A=
ENST00000588882.1:c.458A= ENSP00000466729.1:p.Lys153=
ENST00000589864.1:n.361A=
NM_000363.4:c.533A= , LRG_432t1:c.533A= NP_000354.4:p.Lys178=
NM_000363.5:c.533A= MANE Select NP_000354.4:p.Lys178=