Canonical Allele Identifier: CA2123452860

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423466_23423488delinsCACACACACACACACACACACAG , CM000676.2:g.23423466_23423488delinsCACACACACACACACACACACAG	GRCh38
NC_000014.8:g.23892675_23892697delinsCACACACACACACACACACACAG , CM000676.1:g.23892675_23892697delinsCACACACACACACACACACACAG	GRCh37
NC_000014.7:g.22962515_22962537delinsCACACACACACACACACACACAG	NCBI36
NG_007884.1:g.17174_17196delinsCTGTGTGTGTGTGTGTGTGTGTG , LRG_384:g.17174_17196delinsCTGTGTGTGTGTGTGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG MANE Select	ENSP00000347507.3:n.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGT...
ENST00000355349.3:c.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG	ENSP00000347507.3:n.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGT...
NM_000257.3:c.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG	NP_000248.2:n.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG
XR_245686.3:n.3205+59_3205+81delinsCTGTGTGTGTGTGTGTGTGTGTG
XM_017021340.1:c.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG	XP_016876829.1:n.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG...
NM_000257.4:c.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG MANE Select	NP_000248.2:n.3099+59_3099+81delinsCTGTGTGTGTGTGTGTGTGTGTG