Canonical Allele Identifier: CA407439492
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151865A>T , CM000681.2:g.55151865A>T GRCh38
NC_000019.9:g.55663233A>T , CM000681.1:g.55663233A>T GRCh37
NC_000019.8:g.60355045A>T NCBI36
NG_007866.2:g.10868T>A , LRG_432:g.10868T>A
NG_011829.2:g.2374T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.602T>A MANE Select ENSP00000341838.5:p.Met201Lys
ENST00000665070.1:c.635T>A ENSP00000499482.1:p.Met212Lys
ENST00000344887.9:c.602T>A ENSP00000341838.5:p.Met201Lys
ENST00000585806.5:n.601T>A
ENST00000588882.1:c.527T>A ENSP00000466729.1:p.Met176Lys
ENST00000589864.1:n.430T>A
NM_000363.4:c.602T>A , LRG_432t1:c.602T>A NP_000354.4:p.Met201Lys
NM_000363.5:c.602T>A MANE Select NP_000354.4:p.Met201Lys