Canonical Allele Identifier: CA2624230050
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23419380-CTG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419384_23419385del , CM000676.2:g.23419384_23419385del GRCh38
NC_000014.8:g.23888593_23888594del , CM000676.1:g.23888593_23888594del GRCh37
NC_000014.7:g.22958433_22958434del NCBI36
NG_007884.1:g.21280_21281del , LRG_384:g.21280_21281del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3854-87_3854-86del MANE Select ENSP00000347507.3:n.3854-87_3854-86del
ENST00000355349.3:c.3854-87_3854-86del ENSP00000347507.3:n.3854-87_3854-86del
NM_000257.3:c.3854-87_3854-86del NP_000248.2:n.3854-87_3854-86del
XM_017021340.1:c.3854-87_3854-86del XP_016876829.1:n.3854-87_3854-86del
NM_000257.4:c.3854-87_3854-86del MANE Select NP_000248.2:n.3854-87_3854-86del
Search 100 bp 5'
Search 100 bp 3'