Canonical Allele Identifier: CA2800863397
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423438_23423442del , CM000676.2:g.23423438_23423442del GRCh38
NC_000014.8:g.23892647_23892651del , CM000676.1:g.23892647_23892651del GRCh37
NC_000014.7:g.22962487_22962491del NCBI36
NG_007884.1:g.17220_17224del , LRG_384:g.17220_17224del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+105_3099+109del MANE Select ENSP00000347507.3:n.3099+105_3099+109del
ENST00000355349.3:c.3099+105_3099+109del ENSP00000347507.3:n.3099+105_3099+109del
NM_000257.3:c.3099+105_3099+109del NP_000248.2:n.3099+105_3099+109del
XR_245686.3:n.3205+105_3205+109del
XM_017021340.1:c.3099+105_3099+109del XP_016876829.1:n.3099+105_3099+109del
NM_000257.4:c.3099+105_3099+109del MANE Select NP_000248.2:n.3099+105_3099+109del