Canonical Allele Identifier: CA2624251036
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431337_23431339del , CM000676.2:g.23431337_23431339del GRCh38
NC_000014.8:g.23900546_23900548del , CM000676.1:g.23900546_23900548del GRCh37
NC_000014.7:g.22970386_22970388del NCBI36
NG_007884.1:g.9324_9326del , LRG_384:g.9324_9326del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.796+80_796+82del MANE Select ENSP00000347507.3:n.796+80_796+82del
ENST00000355349.3:c.796+80_796+82del ENSP00000347507.3:n.796+80_796+82del
NM_000257.3:c.796+80_796+82del NP_000248.2:n.796+80_796+82del
XR_245686.3:n.902+80_902+82del
XM_017021340.1:c.796+80_796+82del XP_016876829.1:n.796+80_796+82del
NM_000257.4:c.796+80_796+82del MANE Select NP_000248.2:n.796+80_796+82del