Canonical Allele Identifier: CA2123462913
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415369_23415370delinsTG , CM000676.2:g.23415369_23415370delinsTG GRCh38
NC_000014.8:g.23884578_23884579delinsTG , CM000676.1:g.23884578_23884579delinsTG GRCh37
NC_000014.7:g.22954418_22954419delinsTG NCBI36
NG_007884.1:g.25292_25293delinsCA , LRG_384:g.25292_25293delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5283+11_5283+12delinsCA MANE Select ENSP00000347507.3:n.5283+11_5283+12delins...
ENST00000355349.3:c.5283+11_5283+12delinsCA ENSP00000347507.3:n.5283+11_5283+12delins...
NM_000257.3:c.5283+11_5283+12delinsCA NP_000248.2:n.5283+11_5283+12delinsCA
XM_017021340.1:c.5283+11_5283+12delinsCA XP_016876829.1:n.5283+11_5283+12delinsCA
NM_000257.4:c.5283+11_5283+12delinsCA MANE Select NP_000248.2:n.5283+11_5283+12delinsCA
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