Canonical Allele Identifier: CA2123458855

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23413920_23413921delinsGA , CM000676.2:g.23413920_23413921delinsGA	GRCh38
NC_000014.8:g.23883129_23883130delinsGA , CM000676.1:g.23883129_23883130delinsGA	GRCh37
NC_000014.7:g.22952969_22952970delinsGA	NCBI36
NG_007884.1:g.26741_26742delinsTC , LRG_384:g.26741_26742delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.5656-28_5656-27delinsTC MANE Select	ENSP00000347507.3:n.5656-28_5656-27delinsTC
ENST00000355349.3:c.5656-28_5656-27delinsTC	ENSP00000347507.3:n.5656-28_5656-27delinsTC
NM_000257.3:c.5656-28_5656-27delinsTC	NP_000248.2:n.5656-28_5656-27delinsTC
XM_017021340.1:c.5656-28_5656-27delinsTC	XP_016876829.1:n.5656-28_5656-27delinsTC
NM_000257.4:c.5656-28_5656-27delinsTC MANE Select	NP_000248.2:n.5656-28_5656-27delinsTC