Canonical Allele Identifier: CA2624239065
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429458_23429459del , CM000676.2:g.23429458_23429459del GRCh38
NC_000014.8:g.23898667_23898668del , CM000676.1:g.23898667_23898668del GRCh37
NC_000014.7:g.22968507_22968508del NCBI36
NG_007884.1:g.11203_11204del , LRG_384:g.11203_11204del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1139-112_1139-111del MANE Select ENSP00000347507.3:n.1139-112_1139-111del
ENST00000355349.3:c.1139-112_1139-111del ENSP00000347507.3:n.1139-112_1139-111del
NM_000257.3:c.1139-112_1139-111del NP_000248.2:n.1139-112_1139-111del
XR_245686.3:n.1245-112_1245-111del
XM_017021340.1:c.1139-112_1139-111del XP_016876829.1:n.1139-112_1139-111del
NM_000257.4:c.1139-112_1139-111del MANE Select NP_000248.2:n.1139-112_1139-111del