Canonical Allele Identifier: CA2123464428

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415778_23415781delinsTCTC , CM000676.2:g.23415778_23415781delinsTCTC GRCh38
NC_000014.8:g.23884987_23884990delinsTCTC , CM000676.1:g.23884987_23884990delinsTCTC GRCh37
NC_000014.7:g.22954827_22954830delinsTCTC NCBI36
NG_007884.1:g.24881_24884delinsGAGA , LRG_384:g.24881_24884delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5005_5008delinsGAGA (MYH7) MANE Select ENSP00000347507.3:p.Glu1669=
ENST00000355349.3:c.5005_5008delinsGAGA (MYH7) ENSP00000347507.3:p.Glu1669=
NM_000257.3:c.5005_5008delinsGAGA (MYH7) NP_000248.2:p.Glu1669=
NR_126491.1:n.210_213delinsTCTC (MHRT)
XM_017021340.1:c.5005_5008delinsGAGA (MYH7) XP_016876829.1:p.Glu1669=
NM_000257.4:c.5005_5008delinsGAGA (MYH7) MANE Select NP_000248.2:p.Glu1669=