Canonical Allele Identifier: CA937656242

Gene: MYBPC3

Linked Data

• gnomAD v3: 11-47343672-T-TCCC
• gnomAD v4: 11-47343672-T-TCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47343675_47343677dup , CM000673.2:g.47343675_47343677dup	GRCh38
NC_000011.9:g.47365226_47365228dup , CM000673.1:g.47365226_47365228dup	GRCh37
NC_000011.8:g.47321802_47321804dup	NCBI36
NG_007667.1:g.14028_14030dup , LRG_386:g.14028_14030dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1091-51_1091-49dup MANE Select	ENSP00000442795.1:n.1091-51_1091-49dup
ENST00000256993.8:c.1091-51_1091-49dup	ENSP00000256993.5:n.1091-51_1091-49dup
ENST00000399249.6:c.1091-51_1091-49dup	ENSP00000382193.2:n.1091-51_1091-49dup
ENST00000544791.1:c.1091-51_1091-49dup	ENSP00000444259.1:n.1091-51_1091-49dup
ENST00000545968.5:c.1091-51_1091-49dup	ENSP00000442795.1:n.1091-51_1091-49dup
NM_000256.3:c.1091-51_1091-49dup , LRG_386t1:c.1091-51_1091-49dup MANE Select	NP_000247.2:n.1091-51_1091-49dup
XM_011520117.1:c.1073-51_1073-49dup	XP_011518419.1:n.1073-51_1073-49dup
XM_011520118.1:c.1091-51_1091-49dup	XP_011518420.1:n.1091-51_1091-49dup