Canonical Allele Identifier: CA1969333713

Gene: MYBPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47332299_47332303delinsTGAGA , CM000673.2:g.47332299_47332303delinsTGAGA	GRCh38
NC_000011.9:g.47353850_47353854delinsTGAGA , CM000673.1:g.47353850_47353854delinsTGAGA	GRCh37
NC_000011.8:g.47310426_47310430delinsTGAGA	NCBI36
NG_007667.1:g.25400_25404delinsTCTCA , LRG_386:g.25400_25404delinsTCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.3628-45_3628-41delinsTCTCA MANE Select	ENSP00000442795.1:n.3628-45_3628-41delinsTCTCA
ENST00000256993.8:c.3628-45_3628-41delinsTCTCA	ENSP00000256993.5:n.3628-45_3628-41delinsTCTCA
ENST00000399249.6:c.3628-45_3628-41delinsTCTCA	ENSP00000382193.2:n.3628-45_3628-41delinsTCTCA
ENST00000545968.5:c.3628-45_3628-41delinsTCTCA	ENSP00000442795.1:n.3628-45_3628-41delinsTCTCA
NM_000256.3:c.3628-45_3628-41delinsTCTCA , LRG_386t1:c.3628-45_3628-41delinsTCTCA MANE Select	NP_000247.2:n.3628-45_3628-41delinsTCTCA
XM_011520117.1:c.3610-45_3610-41delinsTCTCA	XP_011518419.1:n.3610-45_3610-41delinsTCTCA
XM_011520118.1:c.3547-45_3547-41delinsTCTCA	XP_011518420.1:n.3547-45_3547-41delinsTCTCA