Canonical Allele Identifier: CA2814881365
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154833_55154834insCAGCTCCGC , CM000681.2:g.55154833_55154834insCAGCTCCGC GRCh38
NC_000019.9:g.55666201_55666202insCAGCTCCGC , CM000681.1:g.55666201_55666202insCAGCTCCGC GRCh37
NC_000019.8:g.60358013_60358014insCAGCTCCGC NCBI36
NG_007866.2:g.7899_7900insGCGGAGCTG , LRG_432:g.7899_7900insGCGGAGCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.283-4_283-3insGCGGAGCTG MANE Select ENSP00000341838.5:n.283-4_283-3insGCGGAGCTG
ENST00000665070.1:c.283-4_283-3insGCGGAGCTG ENSP00000499482.1:n.283-4_283-3insGCGGAGCTG
ENST00000344887.9:c.283-4_283-3insGCGGAGCTG ENSP00000341838.5:n.283-4_283-3insGCGGAGCTG
ENST00000585806.5:n.282-4_282-3insGCGGAGCTG
ENST00000586669.5:n.291-4_291-3insGCGGAGCTG
ENST00000587176.5:n.467-4_467-3insGCGGAGCTG
ENST00000587871.1:c.902-4_902-3insGCGGAGCTG
ENST00000588882.1:c.208-4_208-3insGCGGAGCTG ENSP00000466729.1:n.208-4_208-3insGCGGAGCTG
ENST00000590463.1:n.455-4_455-3insGCGGAGCTG
NM_000363.4:c.283-4_283-3insGCGGAGCTG , LRG_432t1:c.283-4_283-3insGCGGAGCTG NP_000354.4:n.283-4_283-3insGCGGAGCTG
NM_000363.5:c.283-4_283-3insGCGGAGCTG MANE Select NP_000354.4:n.283-4_283-3insGCGGAGCTG