Canonical Allele Identifier: CA2624254187
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433559_23433560insCC , CM000676.2:g.23433559_23433560insCC GRCh38
NC_000014.8:g.23902768_23902769insCC , CM000676.1:g.23902768_23902769insCC GRCh37
NC_000014.7:g.22972608_22972609insCC NCBI36
NG_007884.1:g.7102_7103insGG , LRG_384:g.7102_7103insGG

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.173_174insGG MANE Select ENSP00000347507.3:p.Val59GlufsTer12
ENST00000355349.3:c.173_174insGG ENSP00000347507.3:p.Val59GlufsTer12
NM_000257.3:c.173_174insGG NP_000248.2:p.Val59GlufsTer12
XR_245686.3:n.279_280insGG
XM_017021340.1:c.173_174insGG XP_016876829.1:p.Val59GlufsTer12
NM_000257.4:c.173_174insGG MANE Select NP_000248.2:p.Val59GlufsTer12