Canonical Allele Identifier: CA2343272532
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151870A= , CM000681.2:g.55151870A= GRCh38
NC_000019.9:g.55663238A= , CM000681.1:g.55663238A= GRCh37
NC_000019.8:g.60355050A= NCBI36
NG_007866.2:g.10863T= , LRG_432:g.10863T=
NG_011829.2:g.2369T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.597T= MANE Select ENSP00000341838.5:p.Ser199=
ENST00000665070.1:c.630T= ENSP00000499482.1:p.Ser210=
ENST00000344887.9:c.597T= ENSP00000341838.5:p.Ser199=
ENST00000585806.5:n.596T=
ENST00000588882.1:c.522T= ENSP00000466729.1:p.Ser174=
ENST00000589864.1:n.425T=
NM_000363.4:c.597T= , LRG_432t1:c.597T= NP_000354.4:p.Ser199=
NM_000363.5:c.597T= MANE Select NP_000354.4:p.Ser199=