Canonical Allele Identifier: CA2534665729
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431197_23431198insTTCCCTCTGCCTTTTGCTTGCTACATTTATCATTA , CM000676.2:g.23431197_23431198insTTCCCTCTGCCTTTTGCTTGCTACATTTATCATTA GRCh38
NC_000014.8:g.23900406_23900407insTTCCCTCTGCCTTTTGCTTGCTACATTTATCATTA , CM000676.1:g.23900406_23900407insTTCCCTCTGCCTTTTGCTTGCTACATTTATCATTA GRCh37
NC_000014.7:g.22970246_22970247insTTCCCTCTGCCTTTTGCTTGCTACATTTATCATTA NCBI36
NG_007884.1:g.9464_9465insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA , LRG_384:g.9464_9465insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA MANE Select ENSP00000347507.3:n.797-199_797-198insTAATGATAAATGTAGCAAGCAAA...
ENST00000355349.3:c.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA ENSP00000347507.3:n.797-199_797-198insTAATGATAAATGTAGCAAGCAAA...
NM_000257.3:c.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA NP_000248.2:n.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGGCAG...
XR_245686.3:n.903-199_903-198insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA
XM_017021340.1:c.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA XP_016876829.1:n.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGG...
NM_000257.4:c.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGGCAGAGGGAA MANE Select NP_000248.2:n.797-199_797-198insTAATGATAAATGTAGCAAGCAAAAGGCAG...