Canonical Allele Identifier: CA2624229959

Gene: MYH7

Linked Data

• gnomAD v4: 14-23425616-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425617del , CM000676.2:g.23425617del	GRCh38
NC_000014.8:g.23894826del , CM000676.1:g.23894826del	GRCh37
NC_000014.7:g.22964666del	NCBI36
NG_007884.1:g.15045del , LRG_384:g.15045del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2286+78del MANE Select	ENSP00000347507.3:n.2286+78del
ENST00000355349.3:c.2286+78del	ENSP00000347507.3:n.2286+78del
NM_000257.3:c.2286+78del	NP_000248.2:n.2286+78del
XR_245686.3:n.2392+78del
XM_017021340.1:c.2286+78del	XP_016876829.1:n.2286+78del
NM_000257.4:c.2286+78del MANE Select	NP_000248.2:n.2286+78del