Canonical Allele Identifier: CA2123458028

Gene: MYH7

Linked Data

• dbSNP Id: rs1892663708
• gnomAD v4: 14-23425633-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425633_23425634insA , CM000676.2:g.23425633_23425634insA	GRCh38
NC_000014.8:g.23894842_23894843insA , CM000676.1:g.23894842_23894843insA	GRCh37
NC_000014.7:g.22964682_22964683insA	NCBI36
NG_007884.1:g.15028_15029insT , LRG_384:g.15028_15029insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2286+61_2286+62insT MANE Select	ENSP00000347507.3:n.2286+61_2286+62insT
ENST00000355349.3:c.2286+61_2286+62insT	ENSP00000347507.3:n.2286+61_2286+62insT
NM_000257.3:c.2286+61_2286+62insT	NP_000248.2:n.2286+61_2286+62insT
XR_245686.3:n.2392+61_2392+62insT
XM_017021340.1:c.2286+61_2286+62insT	XP_016876829.1:n.2286+61_2286+62insT
NM_000257.4:c.2286+61_2286+62insT MANE Select	NP_000248.2:n.2286+61_2286+62insT