Canonical Allele Identifier: CA937656235

Gene: MYBPC3

Linked Data

• gnomAD v3: 11-47343670-G-GCCC
• gnomAD v4: 11-47343670-G-GCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47343671_47343672insCCC , CM000673.2:g.47343671_47343672insCCC	GRCh38
NC_000011.9:g.47365222_47365223insCCC , CM000673.1:g.47365222_47365223insCCC	GRCh37
NC_000011.8:g.47321798_47321799insCCC	NCBI36
NG_007667.1:g.14032_14033insGGG , LRG_386:g.14032_14033insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545968.6:c.1091-47_1091-46insGGG MANE Select	ENSP00000442795.1:n.1091-47_1091-46insGGG
ENST00000256993.8:c.1091-47_1091-46insGGG	ENSP00000256993.5:n.1091-47_1091-46insGGG
ENST00000399249.6:c.1091-47_1091-46insGGG	ENSP00000382193.2:n.1091-47_1091-46insGGG
ENST00000544791.1:c.1091-47_1091-46insGGG	ENSP00000444259.1:n.1091-47_1091-46insGGG
ENST00000545968.5:c.1091-47_1091-46insGGG	ENSP00000442795.1:n.1091-47_1091-46insGGG
NM_000256.3:c.1091-47_1091-46insGGG , LRG_386t1:c.1091-47_1091-46insGGG MANE Select	NP_000247.2:n.1091-47_1091-46insGGG
XM_011520117.1:c.1073-47_1073-46insGGG	XP_011518419.1:n.1073-47_1073-46insGGG
XM_011520118.1:c.1091-47_1091-46insGGG	XP_011518420.1:n.1091-47_1091-46insGGG