Canonical Allele Identifier: CA2575486384

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415744_23415747dup , CM000676.2:g.23415744_23415747dup GRCh38
NC_000014.8:g.23884953_23884956dup , CM000676.1:g.23884953_23884956dup GRCh37
NC_000014.7:g.22954793_22954796dup NCBI36
NG_007884.1:g.24915_24918dup , LRG_384:g.24915_24918dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5039_5042dup (MYH7) MANE Select ENSP00000347507.3:p.Gln1682AlafsTer4
ENST00000355349.3:c.5039_5042dup (MYH7) ENSP00000347507.3:p.Gln1682AlafsTer4
NM_000257.3:c.5039_5042dup (MYH7) NP_000248.2:p.Gln1682AlafsTer4
NR_126491.1:n.176_179dup (MHRT)
XM_017021340.1:c.5039_5042dup (MYH7) XP_016876829.1:p.Gln1682AlafsTer4
NM_000257.4:c.5039_5042dup (MYH7) MANE Select NP_000248.2:p.Gln1682AlafsTer4