Canonical Allele Identifier: CA997246885
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153741_55153747del , CM000681.2:g.55153741_55153747del GRCh38
NC_000019.9:g.55665109_55665115del , CM000681.1:g.55665109_55665115del GRCh37
NC_000019.8:g.60356921_60356927del NCBI36
NG_007866.2:g.8995_9001del , LRG_432:g.8995_9001del
NG_011829.2:g.501_507del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.549+292_549+298del MANE Select ENSP00000341838.5:n.549+292_549+298del
ENST00000665070.1:c.582+292_582+298del ENSP00000499482.1:n.582+292_582+298del
ENST00000344887.9:c.549+292_549+298del ENSP00000341838.5:n.549+292_549+298del
ENST00000585806.5:n.548+292_548+298del
ENST00000588882.1:c.474+292_474+298del ENSP00000466729.1:n.474+292_474+298del
ENST00000589864.1:n.377+292_377+298del
NM_000363.4:c.549+292_549+298del , LRG_432t1:c.549+292_549+298del NP_000354.4:n.549+292_549+298del
NM_000363.5:c.549+292_549+298del MANE Select NP_000354.4:n.549+292_549+298del