Canonical Allele Identifier: CA937656166

Gene: MYBPC3

Linked Data

• gnomAD v3: 11-47343651-A-ACCCCCCCCCCC
• gnomAD v4: 11-47343651-A-ACCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47343655_47343656insCCCCCCCCCCC , CM000673.2:g.47343655_47343656insCCCCCCCCCCC	GRCh38
NC_000011.9:g.47365206_47365207insCCCCCCCCCCC , CM000673.1:g.47365206_47365207insCCCCCCCCCCC	GRCh37
NC_000011.8:g.47321782_47321783insCCCCCCCCCCC	NCBI36
NG_007667.1:g.14051_14052insGGGGGGGGGGG , LRG_386:g.14051_14052insGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1091-28_1091-27insGGGGGGGGGGG MANE Select	ENSP00000442795.1:n.1091-28_1091-27insGGGGGGGGGGG
ENST00000256993.8:c.1091-28_1091-27insGGGGGGGGGGG	ENSP00000256993.5:n.1091-28_1091-27insGGGGGGGGGGG
ENST00000399249.6:c.1091-28_1091-27insGGGGGGGGGGG	ENSP00000382193.2:n.1091-28_1091-27insGGGGGGGGGGG
ENST00000544791.1:c.1091-28_1091-27insGGGGGGGGGGG	ENSP00000444259.1:n.1091-28_1091-27insGGGGGGGGGGG
ENST00000545968.5:c.1091-28_1091-27insGGGGGGGGGGG	ENSP00000442795.1:n.1091-28_1091-27insGGGGGGGGGGG
NM_000256.3:c.1091-28_1091-27insGGGGGGGGGGG , LRG_386t1:c.1091-28_1091-27insGGGGGGGGGGG MANE Select	NP_000247.2:n.1091-28_1091-27insGGGGGGGGGGG
XM_011520117.1:c.1073-28_1073-27insGGGGGGGGGGG	XP_011518419.1:n.1073-28_1073-27insGGGGGGGGGGG
XM_011520118.1:c.1091-28_1091-27insGGGGGGGGGGG	XP_011518420.1:n.1091-28_1091-27insGGGGGGGGGGG