Canonical Allele Identifier: CA2624251602
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23431692-AAGG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431696_23431698del , CM000676.2:g.23431696_23431698del GRCh38
NC_000014.8:g.23900905_23900907del , CM000676.1:g.23900905_23900907del GRCh37
NC_000014.7:g.22970745_22970747del NCBI36
NG_007884.1:g.8967_8969del , LRG_384:g.8967_8969del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.640-18_640-16del MANE Select ENSP00000347507.3:n.640-18_640-16del
ENST00000355349.3:c.640-18_640-16del ENSP00000347507.3:n.640-18_640-16del
NM_000257.3:c.640-18_640-16del NP_000248.2:n.640-18_640-16del
XR_245686.3:n.746-18_746-16del
XM_017021340.1:c.640-18_640-16del XP_016876829.1:n.640-18_640-16del
NM_000257.4:c.640-18_640-16del MANE Select NP_000248.2:n.640-18_640-16del
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