Canonical Allele Identifier: CA2123451722
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431480_23431481delinsCC , CM000676.2:g.23431480_23431481delinsCC GRCh38
NC_000014.8:g.23900689_23900690delinsCC , CM000676.1:g.23900689_23900690delinsCC GRCh37
NC_000014.7:g.22970529_22970530delinsCC NCBI36
NG_007884.1:g.9181_9182delinsGG , LRG_384:g.9181_9182delinsGG

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.733_734delinsGG MANE Select ENSP00000347507.3:p.Gly245=
ENST00000355349.3:c.733_734delinsGG ENSP00000347507.3:p.Gly245=
NM_000257.3:c.733_734delinsGG NP_000248.2:p.Gly245=
XR_245686.3:n.839_840delinsGG
XM_017021340.1:c.733_734delinsGG XP_016876829.1:p.Gly245=
NM_000257.4:c.733_734delinsGG MANE Select NP_000248.2:p.Gly245=