Canonical Allele Identifier: CA1969336514
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47342985_47342986delinsTC , CM000673.2:g.47342985_47342986delinsTC GRCh38
NC_000011.9:g.47364536_47364537delinsTC , CM000673.1:g.47364536_47364537delinsTC GRCh37
NC_000011.8:g.47321112_47321113delinsTC NCBI36
NG_007667.1:g.14717_14718delinsGA , LRG_386:g.14717_14718delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.1351+35_1351+36delinsGA MANE Select ENSP00000442795.1:n.1351+35_1351+36delins...
ENST00000256993.8:c.1351+35_1351+36delinsGA ENSP00000256993.5:n.1351+35_1351+36delins...
ENST00000399249.6:c.1351+35_1351+36delinsGA ENSP00000382193.2:n.1351+35_1351+36delins...
ENST00000544791.1:c.1351+35_1351+36delinsGA ENSP00000444259.1:n.1351+35_1351+36delins...
ENST00000545968.5:c.1351+35_1351+36delinsGA ENSP00000442795.1:n.1351+35_1351+36delins...
NM_000256.3:c.1351+35_1351+36delinsGA , LRG_386t1:c.1351+35_1351+36delinsGA MANE Select NP_000247.2:n.1351+35_1351+36delinsGA
XM_011520117.1:c.1333+35_1333+36delinsGA XP_011518419.1:n.1333+35_1333+36delinsGA
XM_011520118.1:c.1351+35_1351+36delinsGA XP_011518420.1:n.1351+35_1351+36delinsGA