Canonical Allele Identifier: CA2576190909

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159177_18159178del , CM000679.2:g.18159177_18159178del	GRCh38
NC_000017.10:g.18062491_18062492del , CM000679.1:g.18062491_18062492del	GRCh37
NC_000017.9:g.18003216_18003217del	NCBI36
NG_011634.1:g.55472_55473del
NG_011634.2:g.55472_55473del

Transcript Alleles

HGVS	Amino-acid change
ENST00000642418.1:n.1495-98_1495-97del
ENST00000643693.1:n.959-98_959-97del
ENST00000644795.1:c.949-98_949-97del	ENSP00000495720.1:n.949-98_949-97del
ENST00000646782.1:n.1891-98_1891-97del
ENST00000647165.2:c.9157-98_9157-97del MANE Select	ENSP00000495481.1:n.9157-98_9157-97del
ENST00000651214.1:n.1662-98_1662-97del
ENST00000205890.9:c.9157-98_9157-97del	ENSP00000205890.5:n.9157-98_9157-97del
ENST00000418233.7:c.949-98_949-97del	ENSP00000408800.3:n.949-98_949-97del
ENST00000433411.7:n.94-98_94-97del
ENST00000445289.6:n.316+1277_316+1278del
ENST00000556535.5:c.19-98_19-97del	ENSP00000451782.1:n.19-98_19-97del
ENST00000557190.5:n.59-98_59-97del
ENST00000557655.5:c.19-98_19-97del	ENSP00000451925.1:n.19-98_19-97del
ENST00000578472.5:c.19-98_19-97del	ENSP00000467989.1:n.19-98_19-97del
ENST00000615845.4:c.9157-98_9157-97del	ENSP00000481642.1:n.9157-98_9157-97del
NM_016239.3:c.9157-98_9157-97del	NP_057323.3:n.9157-98_9157-97del
XM_011523921.1:c.9151-98_9151-97del	XP_011522223.1:n.9151-98_9151-97del
XM_017024714.2:c.9097-98_9097-97del	XP_016880203.1:n.9097-98_9097-97del
XM_017024715.2:c.9160-98_9160-97del	XP_016880204.1:n.9160-98_9160-97del
NM_016239.4:c.9157-98_9157-97del MANE Select	NP_057323.3:n.9157-98_9157-97del