Canonical Allele Identifier: CA2575486873
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23427565del , CM000676.2:g.23427565del GRCh38
NC_000014.8:g.23896774del , CM000676.1:g.23896774del GRCh37
NC_000014.7:g.22966614del NCBI36
NG_007884.1:g.13099del , LRG_384:g.13099del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1888+22del MANE Select ENSP00000347507.3:n.1888+22del
ENST00000355349.3:c.1888+22del ENSP00000347507.3:n.1888+22del
NM_000257.3:c.1888+22del NP_000248.2:n.1888+22del
XR_245686.3:n.1994+22del
XM_017021340.1:c.1888+22del XP_016876829.1:n.1888+22del
NM_000257.4:c.1888+22del MANE Select NP_000248.2:n.1888+22del