Canonical Allele Identifier: CA2250874768

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159301A= , CM000679.2:g.18159301A=	GRCh38
NC_000017.10:g.18062615A= , CM000679.1:g.18062615A=	GRCh37
NC_000017.9:g.18003340A=	NCBI36
NG_011634.1:g.55596A=
NG_011634.2:g.55596A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1521A=
ENST00000643693.1:n.985A=
ENST00000644795.1:c.975A=	ENSP00000495720.1:p.Glu325=
ENST00000646782.1:n.1917A=
ENST00000647165.2:c.9183A= MANE Select	ENSP00000495481.1:p.Glu3061=
ENST00000651214.1:n.1688A=
ENST00000205890.9:c.9183A=	ENSP00000205890.5:p.Glu3061=
ENST00000418233.7:c.975A=	ENSP00000408800.3:p.Glu325=
ENST00000433411.7:n.120A=
ENST00000445289.6:n.316+1401A=
ENST00000556535.5:c.45A=	ENSP00000451782.1:p.Glu15=
ENST00000557190.5:n.85A=
ENST00000557655.5:c.45A=	ENSP00000451925.1:p.Glu15=
ENST00000578472.5:c.45A=	ENSP00000467989.1:p.Glu15=
ENST00000615845.4:c.9183A=	ENSP00000481642.1:p.Glu3061=
NM_016239.3:c.9183A=	NP_057323.3:p.Glu3061=
XM_011523921.1:c.9177A=	XP_011522223.1:p.Glu3059=
XM_017024714.2:c.9123A=	XP_016880203.1:p.Glu3041=
XM_017024715.2:c.9186A=	XP_016880204.1:p.Glu3062=
NM_016239.4:c.9183A= MANE Select	NP_057323.3:p.Glu3061=