Canonical Allele Identifier: CA2123450699

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431017_23431018delinsGA , CM000676.2:g.23431017_23431018delinsGA	GRCh38
NC_000014.8:g.23900226_23900227delinsGA , CM000676.1:g.23900226_23900227delinsGA	GRCh37
NC_000014.7:g.22970066_22970067delinsGA	NCBI36
NG_007884.1:g.9644_9645delinsTC , LRG_384:g.9644_9645delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-19_797-18delinsTC MANE Select	ENSP00000347507.3:n.797-19_797-18delinsTC
ENST00000355349.3:c.797-19_797-18delinsTC	ENSP00000347507.3:n.797-19_797-18delinsTC
NM_000257.3:c.797-19_797-18delinsTC	NP_000248.2:n.797-19_797-18delinsTC
XR_245686.3:n.903-19_903-18delinsTC
XM_017021340.1:c.797-19_797-18delinsTC	XP_016876829.1:n.797-19_797-18delinsTC
NM_000257.4:c.797-19_797-18delinsTC MANE Select	NP_000248.2:n.797-19_797-18delinsTC