Canonical Allele Identifier: CA2800863552

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419455_23419456insG , CM000676.2:g.23419455_23419456insG	GRCh38
NC_000014.8:g.23888664_23888665insG , CM000676.1:g.23888664_23888665insG	GRCh37
NC_000014.7:g.22958504_22958505insG	NCBI36
NG_007884.1:g.21206_21207insC , LRG_384:g.21206_21207insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3853+27_3853+28insC MANE Select	ENSP00000347507.3:n.3853+27_3853+28insC
ENST00000355349.3:c.3853+27_3853+28insC	ENSP00000347507.3:n.3853+27_3853+28insC
NM_000257.3:c.3853+27_3853+28insC	NP_000248.2:n.3853+27_3853+28insC
XM_017021340.1:c.3853+27_3853+28insC	XP_016876829.1:n.3853+27_3853+28insC
NM_000257.4:c.3853+27_3853+28insC MANE Select	NP_000248.2:n.3853+27_3853+28insC