Canonical Allele Identifier: CA407439372
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151837G>C , CM000681.2:g.55151837G>C GRCh38
NC_000019.9:g.55663205G>C , CM000681.1:g.55663205G>C GRCh37
NC_000019.8:g.60355017G>C NCBI36
NG_007866.2:g.10896C>G , LRG_432:g.10896C>G
NG_011829.2:g.2402C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.630C>G MANE Select ENSP00000341838.5:p.Ser210Arg
ENST00000665070.1:c.663C>G ENSP00000499482.1:p.Ser221Arg
ENST00000344887.9:c.630C>G ENSP00000341838.5:p.Ser210Arg
ENST00000585806.5:n.629C>G
ENST00000588882.1:c.555C>G ENSP00000466729.1:p.Ser185Arg
ENST00000589864.1:n.458C>G
NM_000363.4:c.630C>G , LRG_432t1:c.630C>G NP_000354.4:p.Ser210Arg
NM_000363.5:c.630C>G MANE Select NP_000354.4:p.Ser210Arg