Canonical Allele Identifier: CA2343272805
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55152183_55152203delinsCCATCCACTTCCTGTCTCCCT , CM000681.2:g.55152183_55152203delinsCCATCCACTTCCTGTCTCCCT GRCh38
NC_000019.9:g.55663551_55663571delinsCCATCCACTTCCTGTCTCCCT , CM000681.1:g.55663551_55663571delinsCCATCCACTTCCTGTCTCCCT GRCh37
NC_000019.8:g.60355363_60355383delinsCCATCCACTTCCTGTCTCCCT NCBI36
NG_007866.2:g.10530_10550delinsAGGGAGACAGGAAGTGGATGG , LRG_432:g.10530_10550delinsAGGGAGACAGGAAGTGGATGG
NG_011829.2:g.2036_2056delinsAGGGAGACAGGAAGTGGATGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.550-286_550-266delinsAGGGAGACAGGAAGTGGATGG MANE Select ENSP00000341838.5:n.550-286_550-266delinsAGGGAGACAGGAAGTGGATG...
ENST00000665070.1:c.583-286_583-266delinsAGGGAGACAGGAAGTGGATGG ENSP00000499482.1:n.583-286_583-266delinsAGGGAGACAGGAAGTGGATG...
ENST00000344887.9:c.550-286_550-266delinsAGGGAGACAGGAAGTGGATGG ENSP00000341838.5:n.550-286_550-266delinsAGGGAGACAGGAAGTGGATG...
ENST00000585806.5:n.549-286_549-266delinsAGGGAGACAGGAAGTGGATGG
ENST00000588882.1:c.475-286_475-266delinsAGGGAGACAGGAAGTGGATGG ENSP00000466729.1:n.475-286_475-266delinsAGGGAGACAGGAAGTGGATG...
ENST00000589864.1:n.378-286_378-266delinsAGGGAGACAGGAAGTGGATGG
NM_000363.4:c.550-286_550-266delinsAGGGAGACAGGAAGTGGATGG , LRG_432t1:c.550-286_550-266delinsAGGGAGACAGGAAGTGGATGG NP_000354.4:n.550-286_550-266delinsAGGGAGACAGGAAGTGGATGG
NM_000363.5:c.550-286_550-266delinsAGGGAGACAGGAAGTGGATGG MANE Select NP_000354.4:n.550-286_550-266delinsAGGGAGACAGGAAGTGGATGG