Canonical Allele Identifier: CA2575504428
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423787del , CM000676.2:g.23423787del GRCh38
NC_000014.8:g.23892996del , CM000676.1:g.23892996del GRCh37
NC_000014.7:g.22962836del NCBI36
NG_007884.1:g.16878del , LRG_384:g.16878del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2923-61del MANE Select ENSP00000347507.3:n.2923-61del
ENST00000355349.3:c.2923-61del ENSP00000347507.3:n.2923-61del
NM_000257.3:c.2923-61del NP_000248.2:n.2923-61del
XR_245686.3:n.3029-61del
XM_017021340.1:c.2923-61del XP_016876829.1:n.2923-61del
NM_000257.4:c.2923-61del MANE Select NP_000248.2:n.2923-61del