Canonical Allele Identifier: CA1969339721
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47346381_47346382delinsCA , CM000673.2:g.47346381_47346382delinsCA GRCh38
NC_000011.9:g.47367932_47367933delinsCA , CM000673.1:g.47367932_47367933delinsCA GRCh37
NC_000011.8:g.47324508_47324509delinsCA NCBI36
NG_007667.1:g.11321_11322delinsTG , LRG_386:g.11321_11322delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.927-12_927-11delinsTG MANE Select ENSP00000442795.1:n.927-12_927-11delinsTG...
ENST00000256993.8:c.927-12_927-11delinsTG ENSP00000256993.5:n.927-12_927-11delinsTG...
ENST00000399249.6:c.927-12_927-11delinsTG ENSP00000382193.2:n.927-12_927-11delinsTG...
ENST00000544791.1:c.927-12_927-11delinsTG ENSP00000444259.1:n.927-12_927-11delinsTG...
ENST00000545968.5:c.927-12_927-11delinsTG ENSP00000442795.1:n.927-12_927-11delinsTG...
NM_000256.3:c.927-12_927-11delinsTG , LRG_386t1:c.927-12_927-11delinsTG MANE Select NP_000247.2:n.927-12_927-11delinsTG
XM_011520117.1:c.909-12_909-11delinsTG XP_011518419.1:n.909-12_909-11delinsTG
XM_011520118.1:c.927-12_927-11delinsTG XP_011518420.1:n.927-12_927-11delinsTG