Canonical Allele Identifier: CA2800875463
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433695dup , CM000676.2:g.23433695dup GRCh38
NC_000014.8:g.23902904dup , CM000676.1:g.23902904dup GRCh37
NC_000014.7:g.22972744dup NCBI36
NG_007884.1:g.6971dup , LRG_384:g.6971dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.42dup MANE Select ENSP00000347507.3:p.Tyr15LeufsTer18
ENST00000355349.3:c.42dup ENSP00000347507.3:p.Tyr15LeufsTer18
NM_000257.3:c.42dup NP_000248.2:p.Tyr15LeufsTer18
XR_245686.3:n.148dup
XM_017021340.1:c.42dup XP_016876829.1:p.Tyr15LeufsTer18
NM_000257.4:c.42dup MANE Select NP_000248.2:p.Tyr15LeufsTer18