Canonical Allele Identifier: CA407440310
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1344349140

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154075G>T , CM000681.2:g.55154075G>T GRCh38
NC_000019.9:g.55665443G>T , CM000681.1:g.55665443G>T GRCh37
NC_000019.8:g.60357255G>T NCBI36
NG_007866.2:g.8658C>A , LRG_432:g.8658C>A
NG_011829.2:g.164C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.504C>A MANE Select ENSP00000341838.5:p.Asp168Glu
ENST00000665070.1:c.537C>A ENSP00000499482.1:p.Asp179Glu
ENST00000344887.9:c.504C>A ENSP00000341838.5:p.Asp168Glu
ENST00000585806.5:n.503C>A
ENST00000588882.1:c.429C>A ENSP00000466729.1:p.Asp143Glu
ENST00000589864.1:n.332C>A
NM_000363.4:c.504C>A , LRG_432t1:c.504C>A NP_000354.4:p.Asp168Glu
NM_000363.5:c.504C>A MANE Select NP_000354.4:p.Asp168Glu