Canonical Allele Identifier: CA2123451103

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431301_23431303delinsCAG , CM000676.2:g.23431301_23431303delinsCAG	GRCh38
NC_000014.8:g.23900510_23900512delinsCAG , CM000676.1:g.23900510_23900512delinsCAG	GRCh37
NC_000014.7:g.22970350_22970352delinsCAG	NCBI36
NG_007884.1:g.9359_9361delinsCTG , LRG_384:g.9359_9361delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.796+115_796+117delinsCTG MANE Select	ENSP00000347507.3:n.796+115_796+117delins...
ENST00000355349.3:c.796+115_796+117delinsCTG	ENSP00000347507.3:n.796+115_796+117delins...
NM_000257.3:c.796+115_796+117delinsCTG	NP_000248.2:n.796+115_796+117delinsCTG
XR_245686.3:n.902+115_902+117delinsCTG
XM_017021340.1:c.796+115_796+117delinsCTG	XP_016876829.1:n.796+115_796+117delinsCTG...
NM_000257.4:c.796+115_796+117delinsCTG MANE Select	NP_000248.2:n.796+115_796+117delinsCTG