Canonical Allele Identifier: CA014493
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 42727
dbSNP Id: rs397516029

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47332572del , CM000673.2:g.47332572del GRCh38
NC_000011.9:g.47354123del , CM000673.1:g.47354123del GRCh37
NC_000011.8:g.47310699del NCBI36
NG_007667.1:g.25134del , LRG_386:g.25134del

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.3624del MANE Select ENSP00000442795.1:p.Lys1209SerfsTer28
ENST00000256993.8:c.3624del ENSP00000256993.5:p.Lys1209SerfsTer28
ENST00000399249.6:c.3624del ENSP00000382193.2:p.Lys1209SerfsTer28
ENST00000545968.5:c.3624del ENSP00000442795.1:p.Lys1209SerfsTer28
NM_000256.3:c.3624del , LRG_386t1:c.3624del MANE Select NP_000247.2:p.Lys1209SerfsTer28
XM_011520117.1:c.3606del XP_011518419.1:p.Lys1203SerfsTer28
XM_011520118.1:c.3543del XP_011518420.1:p.Lys1182SerfsTer28