Canonical Allele Identifier: CA704290477
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1307960879

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422539del , CM000676.2:g.23422539del GRCh38
NC_000014.8:g.23891748del , CM000676.1:g.23891748del GRCh37
NC_000014.7:g.22961588del NCBI36
NG_007884.1:g.18125del , LRG_384:g.18125del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-212del MANE Select ENSP00000347507.3:n.3100-212del
ENST00000355349.3:c.3100-212del ENSP00000347507.3:n.3100-212del
NM_000257.3:c.3100-212del NP_000248.2:n.3100-212del
XR_245686.3:n.3206-212del
XM_017021340.1:c.3100-212del XP_016876829.1:n.3100-212del
NM_000257.4:c.3100-212del MANE Select NP_000248.2:n.3100-212del