Canonical Allele Identifier: CA2123445956

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419822_23419823delinsAG , CM000676.2:g.23419822_23419823delinsAG	GRCh38
NC_000014.8:g.23889031_23889032delinsAG , CM000676.1:g.23889031_23889032delinsAG	GRCh37
NC_000014.7:g.22958871_22958872delinsAG	NCBI36
NG_007884.1:g.20839_20840delinsCT , LRG_384:g.20839_20840delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3726+22_3726+23delinsCT MANE Select	ENSP00000347507.3:n.3726+22_3726+23delinsCT
ENST00000355349.3:c.3726+22_3726+23delinsCT	ENSP00000347507.3:n.3726+22_3726+23delinsCT
NM_000257.3:c.3726+22_3726+23delinsCT	NP_000248.2:n.3726+22_3726+23delinsCT
XM_017021340.1:c.3726+22_3726+23delinsCT	XP_016876829.1:n.3726+22_3726+23delinsCT
NM_000257.4:c.3726+22_3726+23delinsCT MANE Select	NP_000248.2:n.3726+22_3726+23delinsCT