Canonical Allele Identifier: CA1969336769
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47334918_47334936delinsCCTGTCTCTGCCCAGCGTT , CM000673.2:g.47334918_47334936delinsCCTGTCTCTGCCCAGCGTT GRCh38
NC_000011.9:g.47356469_47356487delinsCCTGTCTCTGCCCAGCGTT , CM000673.1:g.47356469_47356487delinsCCTGTCTCTGCCCAGCGTT GRCh37
NC_000011.8:g.47313045_47313063delinsCCTGTCTCTGCCCAGCGTT NCBI36
NG_007667.1:g.22767_22785delinsAACGCTGGGCAGAGACAGG , LRG_386:g.22767_22785delinsAACGCTGGGCAGAGACAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.2905+106_2905+124delinsAACGCTGGGCAGAGACAGG MANE Select ENSP00000442795.1:n.2905+106_2905+124delinsAACGCTGGGCAGAGACAG...
ENST00000256993.8:c.2905+106_2905+124delinsAACGCTGGGCAGAGACAGG ENSP00000256993.5:n.2905+106_2905+124delinsAACGCTGGGCAGAGACAG...
ENST00000399249.6:c.2905+106_2905+124delinsAACGCTGGGCAGAGACAGG ENSP00000382193.2:n.2905+106_2905+124delinsAACGCTGGGCAGAGACAG...
ENST00000545968.5:c.2905+106_2905+124delinsAACGCTGGGCAGAGACAGG ENSP00000442795.1:n.2905+106_2905+124delinsAACGCTGGGCAGAGACAG...
NM_000256.3:c.2905+106_2905+124delinsAACGCTGGGCAGAGACAGG , LRG_386t1:c.2905+106_2905+124delinsAACGCTGGGCAGAGACAGG MANE Select NP_000247.2:n.2905+106_2905+124delinsAACGCTGGGCAGAGACAGG
XM_011520117.1:c.2887+106_2887+124delinsAACGCTGGGCAGAGACAGG XP_011518419.1:n.2887+106_2887+124delinsAACGCTGGGCAGAGACAGG
XM_011520118.1:c.2824+106_2824+124delinsAACGCTGGGCAGAGACAGG XP_011518420.1:n.2824+106_2824+124delinsAACGCTGGGCAGAGACAGG