Canonical Allele Identifier: CA2624234131
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422161del , CM000676.2:g.23422161del GRCh38
NC_000014.8:g.23891370del , CM000676.1:g.23891370del GRCh37
NC_000014.7:g.22961210del NCBI36
NG_007884.1:g.18501del , LRG_384:g.18501del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3245+19del MANE Select ENSP00000347507.3:n.3245+19del
ENST00000355349.3:c.3245+19del ENSP00000347507.3:n.3245+19del
NM_000257.3:c.3245+19del NP_000248.2:n.3245+19del
XR_245686.3:n.3351+19del
XM_017021340.1:c.3245+19del XP_016876829.1:n.3245+19del
NM_000257.4:c.3245+19del MANE Select NP_000248.2:n.3245+19del