Canonical Allele Identifier: CA2547659871
Gene: JMY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79262006_79262007insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA , CM000667.2:g.79262006_79262007insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA GRCh38
NC_000005.9:g.78557829_78557830insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA , CM000667.1:g.78557829_78557830insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA GRCh37
NC_000005.8:g.78593585_78593586insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396137.5:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA MANE Select ENSP00000379441.4:n.1033-15904_1033-15903insAATCAAACGCGTTGCCT...
ENST00000396137.4:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA ENSP00000379441.4:n.1033-15904_1033-15903insAATCAAACGCGTTGCCT...
NM_152405.4:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA NP_689618.4:n.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGG...
XM_005248430.1:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA XP_005248487.1:n.1033-15904_1033-15903insAATCAAACGCGTTGCCTCAC...
XM_011543155.1:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA XP_011541457.1:n.1033-15904_1033-15903insAATCAAACGCGTTGCCTCAC...
XM_005248430.3:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA XP_005248487.1:n.1033-15904_1033-15903insAATCAAACGCGTTGCCTCAC...
XM_011543155.3:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA XP_011541457.1:n.1033-15904_1033-15903insAATCAAACGCGTTGCCTCAC...
NM_152405.5:c.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGGCTACGGACAGAATCACTGAACTGTCAGACCTAAGCATCCCACTAACAGACATAGTTGCTCAGGTGAGTAGAGTTCTAGCACAGACAGTGACATCA MANE Select NP_689618.4:n.1033-15904_1033-15903insAATCAAACGCGTTGCCTCACCGG...