Canonical Allele Identifier: CA2800875441

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433486_23433487insCCACC , CM000676.2:g.23433486_23433487insCCACC	GRCh38
NC_000014.8:g.23902695_23902696insCCACC , CM000676.1:g.23902695_23902696insCCACC	GRCh37
NC_000014.7:g.22972535_22972536insCCACC	NCBI36
NG_007884.1:g.7175_7176insGGTGG , LRG_384:g.7175_7176insGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.201+45_201+46insGGTGG MANE Select	ENSP00000347507.3:n.201+45_201+46insGGTGG
ENST00000355349.3:c.201+45_201+46insGGTGG	ENSP00000347507.3:n.201+45_201+46insGGTGG
NM_000257.3:c.201+45_201+46insGGTGG	NP_000248.2:n.201+45_201+46insGGTGG
XR_245686.3:n.307+45_307+46insGGTGG
XM_017021340.1:c.201+45_201+46insGGTGG	XP_016876829.1:n.201+45_201+46insGGTGG
NM_000257.4:c.201+45_201+46insGGTGG MANE Select	NP_000248.2:n.201+45_201+46insGGTGG