Canonical Allele Identifier: CA2800863175

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416339_23416340insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGA , CM000676.2:g.23416339_23416340insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGA GRCh38
NC_000014.8:g.23885548_23885549insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGA , CM000676.1:g.23885548_23885549insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGA GRCh37
NC_000014.7:g.22955388_22955389insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGA NCBI36
NG_007884.1:g.24322_24323insTCGCCACCACAGAGGCAGCCGCAATCGAGGC , LRG_384:g.24322_24323insTCGCCACCACAGAGGCAGCCGCAATCGAGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAGGC (MYH7) MANE Select ENSP00000347507.3:n.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCA...
ENST00000355349.3:c.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAGGC (MYH7) ENSP00000347507.3:n.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCA...
NM_000257.3:c.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAGGC (MYH7) NP_000248.2:n.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAG...
NR_126491.1:n.558+42_558+43insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGA (MHRT)
XM_017021340.1:c.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAGGC (MYH7) XP_016876829.1:n.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATC...
NM_000257.4:c.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAGGC (MYH7) MANE Select NP_000248.2:n.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAG...