Canonical Allele Identifier: CA2624232703
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420855del , CM000676.2:g.23420855del GRCh38
NC_000014.8:g.23890064del , CM000676.1:g.23890064del GRCh37
NC_000014.7:g.22959904del NCBI36
NG_007884.1:g.19808del , LRG_384:g.19808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+104del MANE Select ENSP00000347507.3:n.3336+104del
ENST00000355349.3:c.3336+104del ENSP00000347507.3:n.3336+104del
NM_000257.3:c.3336+104del NP_000248.2:n.3336+104del
XR_245686.3:n.3444+104del
XM_017021340.1:c.3336+104del XP_016876829.1:n.3336+104del
NM_000257.4:c.3336+104del MANE Select NP_000248.2:n.3336+104del