Canonical Allele Identifier: CA2624235003
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423398_23423400del , CM000676.2:g.23423398_23423400del GRCh38
NC_000014.8:g.23892607_23892609del , CM000676.1:g.23892607_23892609del GRCh37
NC_000014.7:g.22962447_22962449del NCBI36
NG_007884.1:g.17263_17265del , LRG_384:g.17263_17265del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+148_3099+150del MANE Select ENSP00000347507.3:n.3099+148_3099+150del
ENST00000355349.3:c.3099+148_3099+150del ENSP00000347507.3:n.3099+148_3099+150del
NM_000257.3:c.3099+148_3099+150del NP_000248.2:n.3099+148_3099+150del
XR_245686.3:n.3205+148_3205+150del
XM_017021340.1:c.3099+148_3099+150del XP_016876829.1:n.3099+148_3099+150del
NM_000257.4:c.3099+148_3099+150del MANE Select NP_000248.2:n.3099+148_3099+150del