Canonical Allele Identifier: CA937656164

Gene: MYBPC3

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47343655_47343656insCCCCCCCCC , CM000673.2:g.47343655_47343656insCCCCCCCCC	GRCh38
NC_000011.9:g.47365206_47365207insCCCCCCCCC , CM000673.1:g.47365206_47365207insCCCCCCCCC	GRCh37
NC_000011.8:g.47321782_47321783insCCCCCCCCC	NCBI36
NG_007667.1:g.14051_14052insGGGGGGGGG , LRG_386:g.14051_14052insGGGGGGGGG

Transcript Alleles

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