Canonical Allele Identifier: CA2580087965

Linked Data

ClinVar Variation Id: 1744413
ClinVar RCV Id: RCV002342798

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415828del , CM000676.2:g.23415828del GRCh38
NC_000014.8:g.23885037del , CM000676.1:g.23885037del GRCh37
NC_000014.7:g.22954877del NCBI36
NG_007884.1:g.24836del , LRG_384:g.24836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4960del (MYH7) MANE Select ENSP00000347507.3:p.Gln1654ArgfsTer14
ENST00000355349.3:c.4960del (MYH7) ENSP00000347507.3:p.Gln1654ArgfsTer14
NM_000257.3:c.4960del (MYH7) NP_000248.2:p.Gln1654ArgfsTer14
NR_126491.1:n.260del (MHRT)
XM_017021340.1:c.4960del (MYH7) XP_016876829.1:p.Gln1654ArgfsTer14
NM_000257.4:c.4960del (MYH7) MANE Select NP_000248.2:p.Gln1654ArgfsTer14