Canonical Allele Identifier: CA2575504305
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420905del , CM000676.2:g.23420905del GRCh38
NC_000014.8:g.23890114del , CM000676.1:g.23890114del GRCh37
NC_000014.7:g.22959954del NCBI36
NG_007884.1:g.19760del , LRG_384:g.19760del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+56del MANE Select ENSP00000347507.3:n.3336+56del
ENST00000355349.3:c.3336+56del ENSP00000347507.3:n.3336+56del
NM_000257.3:c.3336+56del NP_000248.2:n.3336+56del
XR_245686.3:n.3444+56del
XM_017021340.1:c.3336+56del XP_016876829.1:n.3336+56del
NM_000257.4:c.3336+56del MANE Select NP_000248.2:n.3336+56del