Canonical Allele Identifier: CA2800863053

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420358_23420359insA , CM000676.2:g.23420358_23420359insA	GRCh38
NC_000014.8:g.23889567_23889568insA , CM000676.1:g.23889567_23889568insA	GRCh37
NC_000014.7:g.22959407_22959408insA	NCBI36
NG_007884.1:g.20303_20304insT , LRG_384:g.20303_20304insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3337-125_3337-124insT MANE Select	ENSP00000347507.3:n.3337-125_3337-124insT
ENST00000355349.3:c.3337-125_3337-124insT	ENSP00000347507.3:n.3337-125_3337-124insT
NM_000257.3:c.3337-125_3337-124insT	NP_000248.2:n.3337-125_3337-124insT
XR_245686.3:n.3445-125_3445-124insT
XM_017021340.1:c.3337-125_3337-124insT	XP_016876829.1:n.3337-125_3337-124insT
NM_000257.4:c.3337-125_3337-124insT MANE Select	NP_000248.2:n.3337-125_3337-124insT