Canonical Allele Identifier: CA2123452629
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423404_23423405delinsTC , CM000676.2:g.23423404_23423405delinsTC GRCh38
NC_000014.8:g.23892613_23892614delinsTC , CM000676.1:g.23892613_23892614delinsTC GRCh37
NC_000014.7:g.22962453_22962454delinsTC NCBI36
NG_007884.1:g.17257_17258delinsGA , LRG_384:g.17257_17258delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+142_3099+143delinsGA MANE Select ENSP00000347507.3:n.3099+142_3099+143delinsGA
ENST00000355349.3:c.3099+142_3099+143delinsGA ENSP00000347507.3:n.3099+142_3099+143delinsGA
NM_000257.3:c.3099+142_3099+143delinsGA NP_000248.2:n.3099+142_3099+143delinsGA
XR_245686.3:n.3205+142_3205+143delinsGA
XM_017021340.1:c.3099+142_3099+143delinsGA XP_016876829.1:n.3099+142_3099+143delinsGA
NM_000257.4:c.3099+142_3099+143delinsGA MANE Select NP_000248.2:n.3099+142_3099+143delinsGA