Canonical Allele Identifier: CA2123465788

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416210_23416213delinsTCTC , CM000676.2:g.23416210_23416213delinsTCTC GRCh38
NC_000014.8:g.23885419_23885422delinsTCTC , CM000676.1:g.23885419_23885422delinsTCTC GRCh37
NC_000014.7:g.22955259_22955262delinsTCTC NCBI36
NG_007884.1:g.24449_24452delinsGAGA , LRG_384:g.24449_24452delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4744_4747delinsGAGA (MYH7) MANE Select ENSP00000347507.3:p.Glu1582=
ENST00000355349.3:c.4744_4747delinsGAGA (MYH7) ENSP00000347507.3:p.Glu1582=
NM_000257.3:c.4744_4747delinsGAGA (MYH7) NP_000248.2:p.Glu1582=
NR_126491.1:n.471_474delinsTCTC (MHRT)
XM_017021340.1:c.4744_4747delinsGAGA (MYH7) XP_016876829.1:p.Glu1582=
NM_000257.4:c.4744_4747delinsGAGA (MYH7) MANE Select NP_000248.2:p.Glu1582=