Canonical Allele Identifier: CA2613397019

Gene: MYBPC3

Linked Data

• gnomAD v4: 11-47340899-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47340899_47340900insA , CM000673.2:g.47340899_47340900insA	GRCh38
NC_000011.9:g.47362450_47362451insA , CM000673.1:g.47362450_47362451insA	GRCh37
NC_000011.8:g.47319026_47319027insA	NCBI36
NG_007667.1:g.16803_16804insT , LRG_386:g.16803_16804insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1927+103_1927+104insT MANE Select	ENSP00000442795.1:n.1927+103_1927+104insT
ENST00000256993.8:c.1927+103_1927+104insT	ENSP00000256993.5:n.1927+103_1927+104insT
ENST00000399249.6:c.1927+103_1927+104insT	ENSP00000382193.2:n.1927+103_1927+104insT
ENST00000544791.1:c.1927+103_1927+104insT	ENSP00000444259.1:n.1927+103_1927+104insT
ENST00000545968.5:c.1927+103_1927+104insT	ENSP00000442795.1:n.1927+103_1927+104insT
NM_000256.3:c.1927+103_1927+104insT , LRG_386t1:c.1927+103_1927+104insT MANE Select	NP_000247.2:n.1927+103_1927+104insT
XM_011520117.1:c.1909+103_1909+104insT	XP_011518419.1:n.1909+103_1909+104insT
XM_011520118.1:c.1927+103_1927+104insT	XP_011518420.1:n.1927+103_1927+104insT