Canonical Allele Identifier: CA2697553842
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2743838
ClinVar RCV Id: RCV003587562

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422257del , CM000676.2:g.23422257del GRCh38
NC_000014.8:g.23891466del , CM000676.1:g.23891466del GRCh37
NC_000014.7:g.22961306del NCBI36
NG_007884.1:g.18407del , LRG_384:g.18407del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3170del MANE Select ENSP00000347507.3:p.Gly1057AlafsTer3
ENST00000355349.3:c.3170del ENSP00000347507.3:p.Gly1057AlafsTer3
NM_000257.3:c.3170del NP_000248.2:p.Gly1057AlafsTer3
XR_245686.3:n.3276del
XM_017021340.1:c.3170del XP_016876829.1:p.Gly1057AlafsTer3
NM_000257.4:c.3170del MANE Select NP_000248.2:p.Gly1057AlafsTer3