Canonical Allele Identifier: CA2825002015
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069322
ClinVar RCV Id: RCV004007866

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47348545del , CM000673.2:g.47348545del GRCh38
NC_000011.9:g.47370096del , CM000673.1:g.47370096del GRCh37
NC_000011.8:g.47326672del NCBI36
NG_007667.1:g.9158del , LRG_386:g.9158del

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.655-4del MANE Select ENSP00000442795.1:n.655-4del
ENST00000256993.8:c.655-4del ENSP00000256993.5:n.655-4del
ENST00000399249.6:c.655-4del ENSP00000382193.2:n.655-4del
ENST00000544791.1:c.655-4del ENSP00000444259.1:n.655-4del
ENST00000545968.5:c.655-4del ENSP00000442795.1:n.655-4del
NM_000256.3:c.655-4del , LRG_386t1:c.655-4del MANE Select NP_000247.2:n.655-4del
XM_011520117.1:c.655-4del XP_011518419.1:n.655-4del
XM_011520118.1:c.655-4del XP_011518420.1:n.655-4del