Canonical Allele Identifier: CA2613392656

Gene: MYBPC3

Linked Data

• gnomAD v4: 11-47346399-G-GGGGAGAGGGAGAGAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47346402_47346403insAGAGGGAGAGAGAGGG , CM000673.2:g.47346402_47346403insAGAGGGAGAGAGAGGG	GRCh38
NC_000011.9:g.47367953_47367954insAGAGGGAGAGAGAGGG , CM000673.1:g.47367953_47367954insAGAGGGAGAGAGAGGG	GRCh37
NC_000011.8:g.47324529_47324530insAGAGGGAGAGAGAGGG	NCBI36
NG_007667.1:g.11303_11304insTCTCTCTCCCTCTCCC , LRG_386:g.11303_11304insTCTCTCTCCCTCTCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000545968.6:c.927-30_927-29insTCTCTCTCCCTCTCCC MANE Select	ENSP00000442795.1:n.927-30_927-29insTCTCTCTCCCTCTCCC
ENST00000256993.8:c.927-30_927-29insTCTCTCTCCCTCTCCC	ENSP00000256993.5:n.927-30_927-29insTCTCTCTCCCTCTCCC
ENST00000399249.6:c.927-30_927-29insTCTCTCTCCCTCTCCC	ENSP00000382193.2:n.927-30_927-29insTCTCTCTCCCTCTCCC
ENST00000544791.1:c.927-30_927-29insTCTCTCTCCCTCTCCC	ENSP00000444259.1:n.927-30_927-29insTCTCTCTCCCTCTCCC
ENST00000545968.5:c.927-30_927-29insTCTCTCTCCCTCTCCC	ENSP00000442795.1:n.927-30_927-29insTCTCTCTCCCTCTCCC
NM_000256.3:c.927-30_927-29insTCTCTCTCCCTCTCCC , LRG_386t1:c.927-30_927-29insTCTCTCTCCCTCTCCC MANE Select	NP_000247.2:n.927-30_927-29insTCTCTCTCCCTCTCCC
XM_011520117.1:c.909-30_909-29insTCTCTCTCCCTCTCCC	XP_011518419.1:n.909-30_909-29insTCTCTCTCCCTCTCCC
XM_011520118.1:c.927-30_927-29insTCTCTCTCCCTCTCCC	XP_011518420.1:n.927-30_927-29insTCTCTCTCCCTCTCCC