Canonical Allele Identifier: CA2250855927

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154093G= , CM000679.2:g.18154093G=	GRCh38
NC_000017.10:g.18057407G= , CM000679.1:g.18057407G=	GRCh37
NC_000017.9:g.17998132G=	NCBI36
NG_011634.1:g.50388G=
NG_011634.2:g.50388G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644795.1:c.-120-38G=	ENSP00000495720.1:n.-120-38G=
ENST00000646782.1:n.244-38G=
ENST00000647165.2:c.8089-38G= MANE Select	ENSP00000495481.1:n.8089-38G=
ENST00000651214.1:n.235-38G=
ENST00000205890.9:c.8089-38G=	ENSP00000205890.5:n.8089-38G=
ENST00000418233.7:c.-120-38G=	ENSP00000408800.3:n.-120-38G=
ENST00000445289.6:n.40G=
ENST00000536811.5:n.40G=
ENST00000585180.1:c.-158G=	ENSP00000464462.1:n.-158G=
ENST00000615845.4:c.8089-38G=	ENSP00000481642.1:n.8089-38G=
NM_016239.3:c.8089-38G=	NP_057323.3:n.8089-38G=
XM_011523921.1:c.8083-38G=	XP_011522223.1:n.8083-38G=
XM_017024714.2:c.8029-38G=	XP_016880203.1:n.8029-38G=
XM_017024715.2:c.8092-38G=	XP_016880204.1:n.8092-38G=
XR_001752809.1:n.297+47C=
XR_001752810.1:n.297+47C=
NM_016239.4:c.8089-38G= MANE Select	NP_057323.3:n.8089-38G=