Canonical Allele Identifier: CA310146210
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs201521806

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153962_55153963insTAGGC , CM000681.2:g.55153962_55153963insTAGGC GRCh38
NC_000019.9:g.55665330_55665331insTAGGC , CM000681.1:g.55665330_55665331insTAGGC GRCh37
NC_000019.8:g.60357142_60357143insTAGGC NCBI36
NG_007866.2:g.8774_8775insAGCCT , LRG_432:g.8774_8775insAGCCT
NG_011829.2:g.280_281insAGCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+71_549+72insAGCCT MANE Select ENSP00000341838.5:n.549+71_549+72insAGCCT...
ENST00000665070.1:c.582+71_582+72insAGCCT ENSP00000499482.1:n.582+71_582+72insAGCCT...
ENST00000344887.9:c.549+71_549+72insAGCCT ENSP00000341838.5:n.549+71_549+72insAGCCT...
ENST00000585806.5:n.548+71_548+72insAGCCT
ENST00000588882.1:c.474+71_474+72insAGCCT ENSP00000466729.1:n.474+71_474+72insAGCCT...
ENST00000589864.1:n.377+71_377+72insAGCCT
NM_000363.4:c.549+71_549+72insAGCCT , LRG_432t1:c.549+71_549+72insAGCCT NP_000354.4:n.549+71_549+72insAGCCT
NM_000363.5:c.549+71_549+72insAGCCT MANE Select NP_000354.4:n.549+71_549+72insAGCCT