Canonical Allele Identifier: CA2624235612
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423478_23423489del , CM000676.2:g.23423478_23423489del GRCh38
NC_000014.8:g.23892687_23892698del , CM000676.1:g.23892687_23892698del GRCh37
NC_000014.7:g.22962527_22962538del NCBI36
NG_007884.1:g.17174_17185del , LRG_384:g.17174_17185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+59_3099+70del MANE Select ENSP00000347507.3:n.3099+59_3099+70del
ENST00000355349.3:c.3099+59_3099+70del ENSP00000347507.3:n.3099+59_3099+70del
NM_000257.3:c.3099+59_3099+70del NP_000248.2:n.3099+59_3099+70del
XR_245686.3:n.3205+59_3205+70del
XM_017021340.1:c.3099+59_3099+70del XP_016876829.1:n.3099+59_3099+70del
NM_000257.4:c.3099+59_3099+70del MANE Select NP_000248.2:n.3099+59_3099+70del