Canonical Allele Identifier: CA2624255172
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433849_23433858del , CM000676.2:g.23433849_23433858del GRCh38
NC_000014.8:g.23903058_23903067del , CM000676.1:g.23903058_23903067del GRCh37
NC_000014.7:g.22972898_22972907del NCBI36
NG_007884.1:g.6808_6817del , LRG_384:g.6808_6817del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-8-114_-8-105del MANE Select ENSP00000347507.3:n.-8-114_-8-105del
ENST00000355349.3:c.-8-114_-8-105del ENSP00000347507.3:n.-8-114_-8-105del
NM_000257.3:c.-8-114_-8-105del NP_000248.2:n.-8-114_-8-105del
XR_245686.3:n.99-114_99-105del
XM_017021340.1:c.-8-114_-8-105del XP_016876829.1:n.-8-114_-8-105del
NM_000257.4:c.-8-114_-8-105del MANE Select NP_000248.2:n.-8-114_-8-105del