Canonical Allele Identifier: CA2808665079

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159452_18159453insACA , CM000679.2:g.18159452_18159453insACA	GRCh38
NC_000017.10:g.18062766_18062767insACA , CM000679.1:g.18062766_18062767insACA	GRCh37
NC_000017.9:g.18003491_18003492insACA	NCBI36
NG_011634.1:g.55747_55748insACA
NG_011634.2:g.55747_55748insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1567+105_1567+106insACA
ENST00000643693.1:n.1031+105_1031+106insACA
ENST00000644795.1:c.1021+105_1021+106insACA	ENSP00000495720.1:n.1021+105_1021+106insACA
ENST00000646782.1:n.1963+105_1963+106insACA
ENST00000647165.2:c.9229+105_9229+106insACA MANE Select	ENSP00000495481.1:n.9229+105_9229+106insACA
ENST00000651214.1:n.1734+105_1734+106insACA
ENST00000205890.9:c.9229+105_9229+106insACA	ENSP00000205890.5:n.9229+105_9229+106insACA
ENST00000418233.7:c.1021+105_1021+106insACA	ENSP00000408800.3:n.1021+105_1021+106insACA
ENST00000433411.7:n.271_272insACA
ENST00000445289.6:n.316+1552_316+1553insACA
ENST00000556535.5:c.91+105_91+106insACA	ENSP00000451782.1:n.91+105_91+106insACA
ENST00000557190.5:n.131+105_131+106insACA
ENST00000557655.5:c.91+105_91+106insACA	ENSP00000451925.1:n.91+105_91+106insACA
ENST00000578472.5:c.91+105_91+106insACA	ENSP00000467989.1:n.91+105_91+106insACA
ENST00000615845.4:c.9229+105_9229+106insACA	ENSP00000481642.1:n.9229+105_9229+106insACA
NM_016239.3:c.9229+105_9229+106insACA	NP_057323.3:n.9229+105_9229+106insACA
XM_011523921.1:c.9223+105_9223+106insACA	XP_011522223.1:n.9223+105_9223+106insACA
XM_017024714.2:c.9169+105_9169+106insACA	XP_016880203.1:n.9169+105_9169+106insACA
XM_017024715.2:c.9232+105_9232+106insACA	XP_016880204.1:n.9232+105_9232+106insACA
NM_016239.4:c.9229+105_9229+106insACA MANE Select	NP_057323.3:n.9229+105_9229+106insACA