Canonical Allele Identifier: CA1969334771
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47341252_47341254delinsGGA , CM000673.2:g.47341252_47341254delinsGGA GRCh38
NC_000011.9:g.47362803_47362805delinsGGA , CM000673.1:g.47362803_47362805delinsGGA GRCh37
NC_000011.8:g.47319379_47319381delinsGGA NCBI36
NG_007667.1:g.16449_16451delinsTCC , LRG_386:g.16449_16451delinsTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.1791-10_1791-8delinsTCC MANE Select ENSP00000442795.1:n.1791-10_1791-8delinsT...
ENST00000256993.8:c.1791-10_1791-8delinsTCC ENSP00000256993.5:n.1791-10_1791-8delinsT...
ENST00000399249.6:c.1791-10_1791-8delinsTCC ENSP00000382193.2:n.1791-10_1791-8delinsT...
ENST00000544791.1:c.1791-10_1791-8delinsTCC ENSP00000444259.1:n.1791-10_1791-8delinsT...
ENST00000545968.5:c.1791-10_1791-8delinsTCC ENSP00000442795.1:n.1791-10_1791-8delinsT...
NM_000256.3:c.1791-10_1791-8delinsTCC , LRG_386t1:c.1791-10_1791-8delinsTCC MANE Select NP_000247.2:n.1791-10_1791-8delinsTCC
XM_011520117.1:c.1773-10_1773-8delinsTCC XP_011518419.1:n.1773-10_1773-8delinsTCC
XM_011520118.1:c.1791-10_1791-8delinsTCC XP_011518420.1:n.1791-10_1791-8delinsTCC