Canonical Allele Identifier: CA2624230017

Gene: MYH7

Linked Data

• gnomAD v4: 14-23425659-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425659_23425660insG , CM000676.2:g.23425659_23425660insG	GRCh38
NC_000014.8:g.23894868_23894869insG , CM000676.1:g.23894868_23894869insG	GRCh37
NC_000014.7:g.22964708_22964709insG	NCBI36
NG_007884.1:g.15002_15003insC , LRG_384:g.15002_15003insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2286+35_2286+36insC MANE Select	ENSP00000347507.3:n.2286+35_2286+36insC
ENST00000355349.3:c.2286+35_2286+36insC	ENSP00000347507.3:n.2286+35_2286+36insC
NM_000257.3:c.2286+35_2286+36insC	NP_000248.2:n.2286+35_2286+36insC
XR_245686.3:n.2392+35_2392+36insC
XM_017021340.1:c.2286+35_2286+36insC	XP_016876829.1:n.2286+35_2286+36insC
NM_000257.4:c.2286+35_2286+36insC MANE Select	NP_000248.2:n.2286+35_2286+36insC