Canonical Allele Identifier: CA1969331687

Gene: MYBPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47337913_47337915delinsCAA , CM000673.2:g.47337913_47337915delinsCAA	GRCh38
NC_000011.9:g.47359464_47359466delinsCAA , CM000673.1:g.47359464_47359466delinsCAA	GRCh37
NC_000011.8:g.47316040_47316042delinsCAA	NCBI36
NG_007667.1:g.19788_19790delinsTTG , LRG_386:g.19788_19790delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.2309-121_2309-119delinsTTG MANE Select	ENSP00000442795.1:n.2309-121_2309-119delinsTTG
ENST00000256993.8:c.2309-121_2309-119delinsTTG	ENSP00000256993.5:n.2309-121_2309-119delinsTTG
ENST00000399249.6:c.2309-121_2309-119delinsTTG	ENSP00000382193.2:n.2309-121_2309-119delinsTTG
ENST00000544791.1:c.2309-121_2309-119delinsTTG	ENSP00000444259.1:n.2309-121_2309-119delinsTTG
ENST00000545968.5:c.2309-121_2309-119delinsTTG	ENSP00000442795.1:n.2309-121_2309-119delinsTTG
NM_000256.3:c.2309-121_2309-119delinsTTG , LRG_386t1:c.2309-121_2309-119delinsTTG MANE Select	NP_000247.2:n.2309-121_2309-119delinsTTG
XM_011520117.1:c.2291-121_2291-119delinsTTG	XP_011518419.1:n.2291-121_2291-119delinsTTG
XM_011520118.1:c.2228-121_2228-119delinsTTG	XP_011518420.1:n.2228-121_2228-119delinsTTG