Canonical Allele Identifier: CA2123448437
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420884_23420885delinsAC , CM000676.2:g.23420884_23420885delinsAC GRCh38
NC_000014.8:g.23890093_23890094delinsAC , CM000676.1:g.23890093_23890094delinsAC GRCh37
NC_000014.7:g.22959933_22959934delinsAC NCBI36
NG_007884.1:g.19777_19778delinsGT , LRG_384:g.19777_19778delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+73_3336+74delinsGT MANE Select ENSP00000347507.3:n.3336+73_3336+74delinsGT
ENST00000355349.3:c.3336+73_3336+74delinsGT ENSP00000347507.3:n.3336+73_3336+74delinsGT
NM_000257.3:c.3336+73_3336+74delinsGT NP_000248.2:n.3336+73_3336+74delinsGT
XR_245686.3:n.3444+73_3444+74delinsGT
XM_017021340.1:c.3336+73_3336+74delinsGT XP_016876829.1:n.3336+73_3336+74delinsGT
NM_000257.4:c.3336+73_3336+74delinsGT MANE Select NP_000248.2:n.3336+73_3336+74delinsGT