Canonical Allele Identifier: CA2123450946
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431190_23431192delinsGAA , CM000676.2:g.23431190_23431192delinsGAA GRCh38
NC_000014.8:g.23900399_23900401delinsGAA , CM000676.1:g.23900399_23900401delinsGAA GRCh37
NC_000014.7:g.22970239_22970241delinsGAA NCBI36
NG_007884.1:g.9470_9472delinsTTC , LRG_384:g.9470_9472delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-193_797-191delinsTTC MANE Select ENSP00000347507.3:n.797-193_797-191delinsTTC
ENST00000355349.3:c.797-193_797-191delinsTTC ENSP00000347507.3:n.797-193_797-191delinsTTC
NM_000257.3:c.797-193_797-191delinsTTC NP_000248.2:n.797-193_797-191delinsTTC
XR_245686.3:n.903-193_903-191delinsTTC
XM_017021340.1:c.797-193_797-191delinsTTC XP_016876829.1:n.797-193_797-191delinsTTC
NM_000257.4:c.797-193_797-191delinsTTC MANE Select NP_000248.2:n.797-193_797-191delinsTTC