Canonical Allele Identifier: CA2123449087
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421169_23421170delinsTG , CM000676.2:g.23421169_23421170delinsTG GRCh38
NC_000014.8:g.23890378_23890379delinsTG , CM000676.1:g.23890378_23890379delinsTG GRCh37
NC_000014.7:g.22960218_22960219delinsTG NCBI36
NG_007884.1:g.19492_19493delinsCA , LRG_384:g.19492_19493delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3246-122_3246-121delinsCA MANE Select ENSP00000347507.3:n.3246-122_3246-121delinsCA
ENST00000355349.3:c.3246-122_3246-121delinsCA ENSP00000347507.3:n.3246-122_3246-121delinsCA
NM_000257.3:c.3246-122_3246-121delinsCA NP_000248.2:n.3246-122_3246-121delinsCA
XR_245686.3:n.3354-122_3354-121delinsCA
XM_017021340.1:c.3246-122_3246-121delinsCA XP_016876829.1:n.3246-122_3246-121delinsCA
NM_000257.4:c.3246-122_3246-121delinsCA MANE Select NP_000248.2:n.3246-122_3246-121delinsCA