Canonical Allele Identifier: CA2123450690

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431015_23431018delinsGAGA , CM000676.2:g.23431015_23431018delinsGAGA	GRCh38
NC_000014.8:g.23900224_23900227delinsGAGA , CM000676.1:g.23900224_23900227delinsGAGA	GRCh37
NC_000014.7:g.22970064_22970067delinsGAGA	NCBI36
NG_007884.1:g.9644_9647delinsTCTC , LRG_384:g.9644_9647delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-19_797-16delinsTCTC MANE Select	ENSP00000347507.3:n.797-19_797-16delinsTCTC
ENST00000355349.3:c.797-19_797-16delinsTCTC	ENSP00000347507.3:n.797-19_797-16delinsTCTC
NM_000257.3:c.797-19_797-16delinsTCTC	NP_000248.2:n.797-19_797-16delinsTCTC
XR_245686.3:n.903-19_903-16delinsTCTC
XM_017021340.1:c.797-19_797-16delinsTCTC	XP_016876829.1:n.797-19_797-16delinsTCTC
NM_000257.4:c.797-19_797-16delinsTCTC MANE Select	NP_000248.2:n.797-19_797-16delinsTCTC