Canonical Allele Identifier: CA1969333631

Gene: MYBPC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47339957_47339965delinsAATACACCC , CM000673.2:g.47339957_47339965delinsAATACACCC	GRCh38
NC_000011.9:g.47361508_47361516delinsAATACACCC , CM000673.1:g.47361508_47361516delinsAATACACCC	GRCh37
NC_000011.8:g.47318084_47318092delinsAATACACCC	NCBI36
NG_007667.1:g.17738_17746delinsGGGTGTATT , LRG_386:g.17738_17746delinsGGGTGTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1928-175_1928-167delinsGGGTGTATT MANE Select	ENSP00000442795.1:n.1928-175_1928-167delinsGGGTGTATT
ENST00000256993.8:c.1928-175_1928-167delinsGGGTGTATT	ENSP00000256993.5:n.1928-175_1928-167delinsGGGTGTATT
ENST00000399249.6:c.1928-175_1928-167delinsGGGTGTATT	ENSP00000382193.2:n.1928-175_1928-167delinsGGGTGTATT
ENST00000544791.1:c.1928-175_1928-167delinsGGGTGTATT	ENSP00000444259.1:n.1928-175_1928-167delinsGGGTGTATT
ENST00000545968.5:c.1928-175_1928-167delinsGGGTGTATT	ENSP00000442795.1:n.1928-175_1928-167delinsGGGTGTATT
NM_000256.3:c.1928-175_1928-167delinsGGGTGTATT , LRG_386t1:c.1928-175_1928-167delinsGGGTGTATT MANE Select	NP_000247.2:n.1928-175_1928-167delinsGGGTGTATT
XM_011520117.1:c.1910-175_1910-167delinsGGGTGTATT	XP_011518419.1:n.1910-175_1910-167delinsGGGTGTATT
XM_011520118.1:c.1928-175_1928-167delinsGGGTGTATT	XP_011518420.1:n.1928-175_1928-167delinsGGGTGTATT