Canonical Allele Identifier: CA2740097720
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3000923
ClinVar RCV Id: RCV003860082

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431880_23431881del , CM000676.2:g.23431880_23431881del GRCh38
NC_000014.8:g.23901089_23901090del , CM000676.1:g.23901089_23901090del GRCh37
NC_000014.7:g.22970929_22970930del NCBI36
NG_007884.1:g.8781_8782del , LRG_384:g.8781_8782del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.531-12_531-11del MANE Select ENSP00000347507.3:n.531-12_531-11del
ENST00000355349.3:c.531-12_531-11del ENSP00000347507.3:n.531-12_531-11del
NM_000257.3:c.531-12_531-11del NP_000248.2:n.531-12_531-11del
XR_245686.3:n.637-12_637-11del
XM_017021340.1:c.531-12_531-11del XP_016876829.1:n.531-12_531-11del
NM_000257.4:c.531-12_531-11del MANE Select NP_000248.2:n.531-12_531-11del