Canonical Allele Identifier: CA1969335165

Gene: MYBPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47341819_47341823delinsGGTCT , CM000673.2:g.47341819_47341823delinsGGTCT	GRCh38
NC_000011.9:g.47363370_47363374delinsGGTCT , CM000673.1:g.47363370_47363374delinsGGTCT	GRCh37
NC_000011.8:g.47319946_47319950delinsGGTCT	NCBI36
NG_007667.1:g.15880_15884delinsAGACC , LRG_386:g.15880_15884delinsAGACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1790+168_1790+172delinsAGACC MANE Select	ENSP00000442795.1:n.1790+168_1790+172delinsAGACC
ENST00000256993.8:c.1790+168_1790+172delinsAGACC	ENSP00000256993.5:n.1790+168_1790+172delinsAGACC
ENST00000399249.6:c.1790+168_1790+172delinsAGACC	ENSP00000382193.2:n.1790+168_1790+172delinsAGACC
ENST00000544791.1:c.1790+168_1790+172delinsAGACC	ENSP00000444259.1:n.1790+168_1790+172delinsAGACC
ENST00000545968.5:c.1790+168_1790+172delinsAGACC	ENSP00000442795.1:n.1790+168_1790+172delinsAGACC
NM_000256.3:c.1790+168_1790+172delinsAGACC , LRG_386t1:c.1790+168_1790+172delinsAGACC MANE Select	NP_000247.2:n.1790+168_1790+172delinsAGACC
XM_011520117.1:c.1772+168_1772+172delinsAGACC	XP_011518419.1:n.1772+168_1772+172delinsAGACC
XM_011520118.1:c.1790+168_1790+172delinsAGACC	XP_011518420.1:n.1790+168_1790+172delinsAGACC