Canonical Allele Identifier: CA2791323375

Gene: MYBPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47342297_47342298insTGG , CM000673.2:g.47342297_47342298insTGG	GRCh38
NC_000011.9:g.47363848_47363849insTGG , CM000673.1:g.47363848_47363849insTGG	GRCh37
NC_000011.8:g.47320424_47320425insTGG	NCBI36
NG_007667.1:g.15405_15406insCCA , LRG_386:g.15405_15406insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1625-142_1625-141insCCA MANE Select	ENSP00000442795.1:n.1625-142_1625-141insCCA
ENST00000256993.8:c.1625-142_1625-141insCCA	ENSP00000256993.5:n.1625-142_1625-141insCCA
ENST00000399249.6:c.1625-142_1625-141insCCA	ENSP00000382193.2:n.1625-142_1625-141insCCA
ENST00000544791.1:c.1625-142_1625-141insCCA	ENSP00000444259.1:n.1625-142_1625-141insCCA
ENST00000545968.5:c.1625-142_1625-141insCCA	ENSP00000442795.1:n.1625-142_1625-141insCCA
NM_000256.3:c.1625-142_1625-141insCCA , LRG_386t1:c.1625-142_1625-141insCCA MANE Select	NP_000247.2:n.1625-142_1625-141insCCA
XM_011520117.1:c.1607-142_1607-141insCCA	XP_011518419.1:n.1607-142_1607-141insCCA
XM_011520118.1:c.1625-142_1625-141insCCA	XP_011518420.1:n.1625-142_1625-141insCCA