Canonical Allele Identifier: CA2250875089
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18159397_18159398delinsAC , CM000679.2:g.18159397_18159398delinsAC GRCh38
NC_000017.10:g.18062711_18062712delinsAC , CM000679.1:g.18062711_18062712delinsAC GRCh37
NC_000017.9:g.18003436_18003437delinsAC NCBI36
NG_011634.1:g.55692_55693delinsAC
NG_011634.2:g.55692_55693delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000642418.1:n.1567+50_1567+51delinsAC
ENST00000643693.1:n.1031+50_1031+51delinsAC
ENST00000644795.1:c.1021+50_1021+51delinsAC ENSP00000495720.1:n.1021+50_1021+51delinsAC
ENST00000646782.1:n.1963+50_1963+51delinsAC
ENST00000647165.2:c.9229+50_9229+51delinsAC MANE Select ENSP00000495481.1:n.9229+50_9229+51delinsAC
ENST00000651214.1:n.1734+50_1734+51delinsAC
ENST00000205890.9:c.9229+50_9229+51delinsAC ENSP00000205890.5:n.9229+50_9229+51delinsAC
ENST00000418233.7:c.1021+50_1021+51delinsAC ENSP00000408800.3:n.1021+50_1021+51delinsAC
ENST00000433411.7:n.216_217delinsAC
ENST00000445289.6:n.316+1497_316+1498delinsAC
ENST00000556535.5:c.91+50_91+51delinsAC ENSP00000451782.1:n.91+50_91+51delinsAC
ENST00000557190.5:n.131+50_131+51delinsAC
ENST00000557655.5:c.91+50_91+51delinsAC ENSP00000451925.1:n.91+50_91+51delinsAC
ENST00000578472.5:c.91+50_91+51delinsAC ENSP00000467989.1:n.91+50_91+51delinsAC
ENST00000615845.4:c.9229+50_9229+51delinsAC ENSP00000481642.1:n.9229+50_9229+51delinsAC
NM_016239.3:c.9229+50_9229+51delinsAC NP_057323.3:n.9229+50_9229+51delinsAC
XM_011523921.1:c.9223+50_9223+51delinsAC XP_011522223.1:n.9223+50_9223+51delinsAC
XM_017024714.2:c.9169+50_9169+51delinsAC XP_016880203.1:n.9169+50_9169+51delinsAC
XM_017024715.2:c.9232+50_9232+51delinsAC XP_016880204.1:n.9232+50_9232+51delinsAC
NM_016239.4:c.9229+50_9229+51delinsAC MANE Select NP_057323.3:n.9229+50_9229+51delinsAC