Canonical Allele Identifier: CA2343272650
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151900T= , CM000681.2:g.55151900T= GRCh38
NC_000019.9:g.55663268T= , CM000681.1:g.55663268T= GRCh37
NC_000019.8:g.60355080T= NCBI36
NG_007866.2:g.10833A= , LRG_432:g.10833A=
NG_011829.2:g.2339A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.567A= MANE Select ENSP00000341838.5:p.Gly189=
ENST00000665070.1:c.600A= ENSP00000499482.1:p.Gly200=
ENST00000344887.9:c.567A= ENSP00000341838.5:p.Gly189=
ENST00000585806.5:n.566A=
ENST00000588882.1:c.492A= ENSP00000466729.1:p.Gly164=
ENST00000589864.1:n.395A=
NM_000363.4:c.567A= , LRG_432t1:c.567A= NP_000354.4:p.Gly189=
NM_000363.5:c.567A= MANE Select NP_000354.4:p.Gly189=