Canonical Allele Identifier: CA407439486
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151863C>T , CM000681.2:g.55151863C>T GRCh38
NC_000019.9:g.55663231C>T , CM000681.1:g.55663231C>T GRCh37
NC_000019.8:g.60355043C>T NCBI36
NG_007866.2:g.10870G>A , LRG_432:g.10870G>A
NG_011829.2:g.2376G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.604G>A MANE Select ENSP00000341838.5:p.Glu202Lys
ENST00000665070.1:c.637G>A ENSP00000499482.1:p.Glu213Lys
ENST00000344887.9:c.604G>A ENSP00000341838.5:p.Glu202Lys
ENST00000585806.5:n.603G>A
ENST00000588882.1:c.529G>A ENSP00000466729.1:p.Glu177Lys
ENST00000589864.1:n.432G>A
NM_000363.4:c.604G>A , LRG_432t1:c.604G>A NP_000354.4:p.Glu202Lys
NM_000363.5:c.604G>A MANE Select NP_000354.4:p.Glu202Lys