Canonical Allele Identifier: CA2624235673
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423483_23423490del , CM000676.2:g.23423483_23423490del GRCh38
NC_000014.8:g.23892692_23892699del , CM000676.1:g.23892692_23892699del GRCh37
NC_000014.7:g.22962532_22962539del NCBI36
NG_007884.1:g.17172_17179del , LRG_384:g.17172_17179del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+57_3099+64del MANE Select ENSP00000347507.3:n.3099+57_3099+64del
ENST00000355349.3:c.3099+57_3099+64del ENSP00000347507.3:n.3099+57_3099+64del
NM_000257.3:c.3099+57_3099+64del NP_000248.2:n.3099+57_3099+64del
XR_245686.3:n.3205+57_3205+64del
XM_017021340.1:c.3099+57_3099+64del XP_016876829.1:n.3099+57_3099+64del
NM_000257.4:c.3099+57_3099+64del MANE Select NP_000248.2:n.3099+57_3099+64del