Canonical Allele Identifier: CA2842917711
Community Standard Title: NM_000257.4(MYH7):c.211dup (p.Val71GlyfsTer28)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433218dup , CM000676.2:g.23433218dup GRCh38
NC_000014.8:g.23902427dup , CM000676.1:g.23902427dup GRCh37
NC_000014.7:g.22972267dup NCBI36
NG_007884.1:g.7444dup , LRG_384:g.7444dup

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.211dup MANE Select NP_000248.2:p.Val71GlyfsTer28
ENST00000355349.4:c.211dup MANE Select ENSP00000347507.3:p.Val71GlyfsTer28
NM_000257.3:c.211dup NP_000248.2:p.Val71GlyfsTer28
ENST00000355349.3:c.211dup ENSP00000347507.3:p.Val71GlyfsTer28
XM_017021340.1:c.211dup XP_016876829.1:p.Val71GlyfsTer28
XR_245686.3:n.317dup