Canonical Allele Identifier: CA2580088030
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2012938
ClinVar RCV Id: RCV002843483

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431878_23431883del , CM000676.2:g.23431878_23431883del GRCh38
NC_000014.8:g.23901087_23901092del , CM000676.1:g.23901087_23901092del GRCh37
NC_000014.7:g.22970927_22970932del NCBI36
NG_007884.1:g.8780_8785del , LRG_384:g.8780_8785del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.531-13_531-8del MANE Select ENSP00000347507.3:n.531-13_531-8del
ENST00000355349.3:c.531-13_531-8del ENSP00000347507.3:n.531-13_531-8del
NM_000257.3:c.531-13_531-8del NP_000248.2:n.531-13_531-8del
XR_245686.3:n.637-13_637-8del
XM_017021340.1:c.531-13_531-8del XP_016876829.1:n.531-13_531-8del
NM_000257.4:c.531-13_531-8del MANE Select NP_000248.2:n.531-13_531-8del