Canonical Allele Identifier: CA2613401292

Gene: MYBPC3

Linked Data

• gnomAD v4: 11-47351200-A-ACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47351200_47351201insCCC , CM000673.2:g.47351200_47351201insCCC	GRCh38
NC_000011.9:g.47372751_47372752insCCC , CM000673.1:g.47372751_47372752insCCC	GRCh37
NC_000011.8:g.47329327_47329328insCCC	NCBI36
NG_007667.1:g.6502_6503insGGG , LRG_386:g.6502_6503insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.292+38_292+39insGGG MANE Select	ENSP00000442795.1:n.292+38_292+39insGGG
ENST00000256993.8:c.292+38_292+39insGGG	ENSP00000256993.5:n.292+38_292+39insGGG
ENST00000399249.6:c.292+38_292+39insGGG	ENSP00000382193.2:n.292+38_292+39insGGG
ENST00000544791.1:c.292+38_292+39insGGG	ENSP00000444259.1:n.292+38_292+39insGGG
ENST00000545968.5:c.292+38_292+39insGGG	ENSP00000442795.1:n.292+38_292+39insGGG
NM_000256.3:c.292+38_292+39insGGG , LRG_386t1:c.292+38_292+39insGGG MANE Select	NP_000247.2:n.292+38_292+39insGGG
XM_011520117.1:c.292+38_292+39insGGG	XP_011518419.1:n.292+38_292+39insGGG
XM_011520118.1:c.292+38_292+39insGGG	XP_011518420.1:n.292+38_292+39insGGG