Canonical Allele Identifier: CA2250874881

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159307C= , CM000679.2:g.18159307C=	GRCh38
NC_000017.10:g.18062621C= , CM000679.1:g.18062621C=	GRCh37
NC_000017.9:g.18003346C=	NCBI36
NG_011634.1:g.55602C=
NG_011634.2:g.55602C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1527C=
ENST00000643693.1:n.991C=
ENST00000644795.1:c.981C=	ENSP00000495720.1:p.Ser327=
ENST00000646782.1:n.1923C=
ENST00000647165.2:c.9189C= MANE Select	ENSP00000495481.1:p.Ser3063=
ENST00000651214.1:n.1694C=
ENST00000205890.9:c.9189C=	ENSP00000205890.5:p.Ser3063=
ENST00000418233.7:c.981C=	ENSP00000408800.3:p.Ser327=
ENST00000433411.7:n.126C=
ENST00000445289.6:n.316+1407C=
ENST00000556535.5:c.51C=	ENSP00000451782.1:p.Ser17=
ENST00000557190.5:n.91C=
ENST00000557655.5:c.51C=	ENSP00000451925.1:p.Ser17=
ENST00000578472.5:c.51C=	ENSP00000467989.1:p.Ser17=
ENST00000615845.4:c.9189C=	ENSP00000481642.1:p.Ser3063=
NM_016239.3:c.9189C=	NP_057323.3:p.Ser3063=
XM_011523921.1:c.9183C=	XP_011522223.1:p.Ser3061=
XM_017024714.2:c.9129C=	XP_016880203.1:p.Ser3043=
XM_017024715.2:c.9192C=	XP_016880204.1:p.Ser3064=
NM_016239.4:c.9189C= MANE Select	NP_057323.3:p.Ser3063=