Canonical Allele Identifier: CA2800863427
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423446del , CM000676.2:g.23423446del GRCh38
NC_000014.8:g.23892655del , CM000676.1:g.23892655del GRCh37
NC_000014.7:g.22962495del NCBI36
NG_007884.1:g.17216del , LRG_384:g.17216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+101del MANE Select ENSP00000347507.3:n.3099+101del
ENST00000355349.3:c.3099+101del ENSP00000347507.3:n.3099+101del
NM_000257.3:c.3099+101del NP_000248.2:n.3099+101del
XR_245686.3:n.3205+101del
XM_017021340.1:c.3099+101del XP_016876829.1:n.3099+101del
NM_000257.4:c.3099+101del MANE Select NP_000248.2:n.3099+101del