Canonical Allele Identifier: CA2123451285

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431389_23431390delinsGC , CM000676.2:g.23431389_23431390delinsGC	GRCh38
NC_000014.8:g.23900598_23900599delinsGC , CM000676.1:g.23900598_23900599delinsGC	GRCh37
NC_000014.7:g.22970438_22970439delinsGC	NCBI36
NG_007884.1:g.9272_9273delinsGC , LRG_384:g.9272_9273delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.796+28_796+29delinsGC MANE Select	ENSP00000347507.3:n.796+28_796+29delinsGC
ENST00000355349.3:c.796+28_796+29delinsGC	ENSP00000347507.3:n.796+28_796+29delinsGC
NM_000257.3:c.796+28_796+29delinsGC	NP_000248.2:n.796+28_796+29delinsGC
XR_245686.3:n.902+28_902+29delinsGC
XM_017021340.1:c.796+28_796+29delinsGC	XP_016876829.1:n.796+28_796+29delinsGC
NM_000257.4:c.796+28_796+29delinsGC MANE Select	NP_000248.2:n.796+28_796+29delinsGC