Canonical Allele Identifier: CA2123455843
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424822_23424825delinsTCTC , CM000676.2:g.23424822_23424825delinsTCTC GRCh38
NC_000014.8:g.23894031_23894034delinsTCTC , CM000676.1:g.23894031_23894034delinsTCTC GRCh37
NC_000014.7:g.22963871_22963874delinsTCTC NCBI36
NG_007884.1:g.15837_15840delinsGAGA , LRG_384:g.15837_15840delinsGAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2623_2626delinsGAGA MANE Select ENSP00000347507.3:p.Glu875=
ENST00000355349.3:c.2623_2626delinsGAGA ENSP00000347507.3:p.Glu875=
NM_000257.3:c.2623_2626delinsGAGA NP_000248.2:p.Glu875=
XR_245686.3:n.2729_2732delinsGAGA
XM_017021340.1:c.2623_2626delinsGAGA XP_016876829.1:p.Glu875=
NM_000257.4:c.2623_2626delinsGAGA MANE Select NP_000248.2:p.Glu875=