Canonical Allele Identifier: CA2791323185
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47339932_47339933insG , CM000673.2:g.47339932_47339933insG GRCh38
NC_000011.9:g.47361483_47361484insG , CM000673.1:g.47361483_47361484insG GRCh37
NC_000011.8:g.47318059_47318060insG NCBI36
NG_007667.1:g.17770_17771insC , LRG_386:g.17770_17771insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.1928-143_1928-142insC MANE Select ENSP00000442795.1:n.1928-143_1928-142insC
ENST00000256993.8:c.1928-143_1928-142insC ENSP00000256993.5:n.1928-143_1928-142insC
ENST00000399249.6:c.1928-143_1928-142insC ENSP00000382193.2:n.1928-143_1928-142insC
ENST00000544791.1:c.1928-143_1928-142insC ENSP00000444259.1:n.1928-143_1928-142insC
ENST00000545968.5:c.1928-143_1928-142insC ENSP00000442795.1:n.1928-143_1928-142insC
NM_000256.3:c.1928-143_1928-142insC , LRG_386t1:c.1928-143_1928-142insC MANE Select NP_000247.2:n.1928-143_1928-142insC
XM_011520117.1:c.1910-143_1910-142insC XP_011518419.1:n.1910-143_1910-142insC
XM_011520118.1:c.1928-143_1928-142insC XP_011518420.1:n.1928-143_1928-142insC