Canonical Allele Identifier: CA997245976
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2085698882

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55152160_55152163del , CM000681.2:g.55152160_55152163del GRCh38
NC_000019.9:g.55663528_55663531del , CM000681.1:g.55663528_55663531del GRCh37
NC_000019.8:g.60355340_60355343del NCBI36
NG_007866.2:g.10573_10576del , LRG_432:g.10573_10576del
NG_011829.2:g.2079_2082del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.550-243_550-240del MANE Select ENSP00000341838.5:n.550-243_550-240del
ENST00000665070.1:c.583-243_583-240del ENSP00000499482.1:n.583-243_583-240del
ENST00000344887.9:c.550-243_550-240del ENSP00000341838.5:n.550-243_550-240del
ENST00000585806.5:n.549-243_549-240del
ENST00000588882.1:c.475-243_475-240del ENSP00000466729.1:n.475-243_475-240del
ENST00000589864.1:n.378-243_378-240del
NM_000363.4:c.550-243_550-240del , LRG_432t1:c.550-243_550-240del NP_000354.4:n.550-243_550-240del
NM_000363.5:c.550-243_550-240del MANE Select NP_000354.4:n.550-243_550-240del