Canonical Allele Identifier: CA1969331783
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47338085_47338087delinsCCT , CM000673.2:g.47338085_47338087delinsCCT GRCh38
NC_000011.9:g.47359636_47359638delinsCCT , CM000673.1:g.47359636_47359638delinsCCT GRCh37
NC_000011.8:g.47316212_47316214delinsCCT NCBI36
NG_007667.1:g.19616_19618delinsAGG , LRG_386:g.19616_19618delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.2309-293_2309-291delinsAGG MANE Select ENSP00000442795.1:n.2309-293_2309-291delinsAGG
ENST00000256993.8:c.2309-293_2309-291delinsAGG ENSP00000256993.5:n.2309-293_2309-291delinsAGG
ENST00000399249.6:c.2309-293_2309-291delinsAGG ENSP00000382193.2:n.2309-293_2309-291delinsAGG
ENST00000544791.1:c.2309-293_2309-291delinsAGG ENSP00000444259.1:n.2309-293_2309-291delinsAGG
ENST00000545968.5:c.2309-293_2309-291delinsAGG ENSP00000442795.1:n.2309-293_2309-291delinsAGG
NM_000256.3:c.2309-293_2309-291delinsAGG , LRG_386t1:c.2309-293_2309-291delinsAGG MANE Select NP_000247.2:n.2309-293_2309-291delinsAGG
XM_011520117.1:c.2291-293_2291-291delinsAGG XP_011518419.1:n.2291-293_2291-291delinsAGG
XM_011520118.1:c.2228-293_2228-291delinsAGG XP_011518420.1:n.2228-293_2228-291delinsAGG