Canonical Allele Identifier: CA1969331705
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47337935_47337939delinsATTTC , CM000673.2:g.47337935_47337939delinsATTTC GRCh38
NC_000011.9:g.47359486_47359490delinsATTTC , CM000673.1:g.47359486_47359490delinsATTTC GRCh37
NC_000011.8:g.47316062_47316066delinsATTTC NCBI36
NG_007667.1:g.19764_19768delinsGAAAT , LRG_386:g.19764_19768delinsGAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.2309-145_2309-141delinsGAAAT MANE Select ENSP00000442795.1:n.2309-145_2309-141delinsGAAAT
ENST00000256993.8:c.2309-145_2309-141delinsGAAAT ENSP00000256993.5:n.2309-145_2309-141delinsGAAAT
ENST00000399249.6:c.2309-145_2309-141delinsGAAAT ENSP00000382193.2:n.2309-145_2309-141delinsGAAAT
ENST00000544791.1:c.2309-145_2309-141delinsGAAAT ENSP00000444259.1:n.2309-145_2309-141delinsGAAAT
ENST00000545968.5:c.2309-145_2309-141delinsGAAAT ENSP00000442795.1:n.2309-145_2309-141delinsGAAAT
NM_000256.3:c.2309-145_2309-141delinsGAAAT , LRG_386t1:c.2309-145_2309-141delinsGAAAT MANE Select NP_000247.2:n.2309-145_2309-141delinsGAAAT
XM_011520117.1:c.2291-145_2291-141delinsGAAAT XP_011518419.1:n.2291-145_2291-141delinsGAAAT
XM_011520118.1:c.2228-145_2228-141delinsGAAAT XP_011518420.1:n.2228-145_2228-141delinsGAAAT