Canonical Allele Identifier: CA1139532448

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415729_23415731del , CM000676.2:g.23415729_23415731del GRCh38
NC_000014.8:g.23884938_23884940del , CM000676.1:g.23884938_23884940del GRCh37
NC_000014.7:g.22954778_22954780del NCBI36
NG_007884.1:g.24935_24937del , LRG_384:g.24935_24937del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5059_5061del (MYH7) MANE Select ENSP00000347507.3:p.Glu1687del
ENST00000355349.3:c.5059_5061del (MYH7) ENSP00000347507.3:p.Glu1687del
NM_000257.3:c.5059_5061del (MYH7) NP_000248.2:p.Glu1687del
NR_126491.1:n.161_163del (MHRT)
XM_017021340.1:c.5059_5061del (MYH7) XP_016876829.1:p.Glu1687del
NM_000257.4:c.5059_5061del (MYH7) MANE Select NP_000248.2:p.Glu1687del