Canonical Allele Identifier: CA2624251659

Gene: MYH7

Linked Data

• gnomAD v4: 14-23431734-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431735del , CM000676.2:g.23431735del	GRCh38
NC_000014.8:g.23900944del , CM000676.1:g.23900944del	GRCh37
NC_000014.7:g.22970784del	NCBI36
NG_007884.1:g.8927del , LRG_384:g.8927del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.639+26del MANE Select	ENSP00000347507.3:n.639+26del
ENST00000355349.3:c.639+26del	ENSP00000347507.3:n.639+26del
NM_000257.3:c.639+26del	NP_000248.2:n.639+26del
XR_245686.3:n.745+26del
XM_017021340.1:c.639+26del	XP_016876829.1:n.639+26del
NM_000257.4:c.639+26del MANE Select	NP_000248.2:n.639+26del