Canonical Allele Identifier: CA2800863171

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416330_23416331insCGGCTATGCCCGTGACCATGGTCATCA , CM000676.2:g.23416330_23416331insCGGCTATGCCCGTGACCATGGTCATCA GRCh38
NC_000014.8:g.23885539_23885540insCGGCTATGCCCGTGACCATGGTCATCA , CM000676.1:g.23885539_23885540insCGGCTATGCCCGTGACCATGGTCATCA GRCh37
NC_000014.7:g.22955379_22955380insCGGCTATGCCCGTGACCATGGTCATCA NCBI36
NG_007884.1:g.24331_24332insTGATGACCATGGTCACGGGCATAGCCG , LRG_384:g.24331_24332insTGATGACCATGGTCACGGGCATAGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG (MYH7) MANE Select ENSP00000347507.3:n.4645-19_4645-18insTGATGACCATGGTCACGGGCATA...
ENST00000355349.3:c.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG (MYH7) ENSP00000347507.3:n.4645-19_4645-18insTGATGACCATGGTCACGGGCATA...
NM_000257.3:c.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG (MYH7) NP_000248.2:n.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG
NR_126491.1:n.558+33_558+34insCGGCTATGCCCGTGACCATGGTCATCA (MHRT)
XM_017021340.1:c.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG (MYH7) XP_016876829.1:n.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCC...
NM_000257.4:c.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG (MYH7) MANE Select NP_000248.2:n.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG