Canonical Allele Identifier: CA407440311
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154076T>A , CM000681.2:g.55154076T>A GRCh38
NC_000019.9:g.55665444T>A , CM000681.1:g.55665444T>A GRCh37
NC_000019.8:g.60357256T>A NCBI36
NG_007866.2:g.8657A>T , LRG_432:g.8657A>T
NG_011829.2:g.163A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.503A>T MANE Select ENSP00000341838.5:p.Asp168Val
ENST00000665070.1:c.536A>T ENSP00000499482.1:p.Asp179Val
ENST00000344887.9:c.503A>T ENSP00000341838.5:p.Asp168Val
ENST00000585806.5:n.502A>T
ENST00000588882.1:c.428A>T ENSP00000466729.1:p.Asp143Val
ENST00000589864.1:n.331A>T
NM_000363.4:c.503A>T , LRG_432t1:c.503A>T NP_000354.4:p.Asp168Val
NM_000363.5:c.503A>T MANE Select NP_000354.4:p.Asp168Val