Canonical Allele Identifier: CA2580087924
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2443032
ClinVar RCV Id: RCV003150877

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415136del , CM000676.2:g.23415136del GRCh38
NC_000014.8:g.23884345del , CM000676.1:g.23884345del GRCh37
NC_000014.7:g.22954185del NCBI36
NG_007884.1:g.25528del , LRG_384:g.25528del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5420del MANE Select ENSP00000347507.3:p.Gly1807AlafsTer?
ENST00000355349.3:c.5420del ENSP00000347507.3:p.Gly1807AlafsTer?
NM_000257.3:c.5420del NP_000248.2:p.Gly1807AlafsTer?
XM_017021340.1:c.5420del XP_016876829.1:p.Gly1807AlafsTer?
NM_000257.4:c.5420del MANE Select NP_000248.2:p.Gly1807AlafsTer?