Canonical Allele Identifier: CA2624235586
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23423472-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423473del , CM000676.2:g.23423473del GRCh38
NC_000014.8:g.23892682del , CM000676.1:g.23892682del GRCh37
NC_000014.7:g.22962522del NCBI36
NG_007884.1:g.17189del , LRG_384:g.17189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+74del MANE Select ENSP00000347507.3:n.3099+74del
ENST00000355349.3:c.3099+74del ENSP00000347507.3:n.3099+74del
NM_000257.3:c.3099+74del NP_000248.2:n.3099+74del
XR_245686.3:n.3205+74del
XM_017021340.1:c.3099+74del XP_016876829.1:n.3099+74del
NM_000257.4:c.3099+74del MANE Select NP_000248.2:n.3099+74del
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