Canonical Allele Identifier: CA2123464339

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415765_23415771delinsACGATGG , CM000676.2:g.23415765_23415771delinsACGATGG GRCh38
NC_000014.8:g.23884974_23884980delinsACGATGG , CM000676.1:g.23884974_23884980delinsACGATGG GRCh37
NC_000014.7:g.22954814_22954820delinsACGATGG NCBI36
NG_007884.1:g.24891_24897delinsCCATCGT , LRG_384:g.24891_24897delinsCCATCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5015_5021delinsCCATCGT (MYH7) MANE Select ENSP00000347507.3:p.Ala1672=
ENST00000355349.3:c.5015_5021delinsCCATCGT (MYH7) ENSP00000347507.3:p.Ala1672=
NM_000257.3:c.5015_5021delinsCCATCGT (MYH7) NP_000248.2:p.Ala1672=
NR_126491.1:n.197_203delinsACGATGG (MHRT)
XM_017021340.1:c.5015_5021delinsCCATCGT (MYH7) XP_016876829.1:p.Ala1672=
NM_000257.4:c.5015_5021delinsCCATCGT (MYH7) MANE Select NP_000248.2:p.Ala1672=