Canonical Allele Identifier: CA2250855951

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154108C= , CM000679.2:g.18154108C=	GRCh38
NC_000017.10:g.18057422C= , CM000679.1:g.18057422C=	GRCh37
NC_000017.9:g.17998147C=	NCBI36
NG_011634.1:g.50403C=
NG_011634.2:g.50403C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644795.1:c.-120-23C=	ENSP00000495720.1:n.-120-23C=
ENST00000646782.1:n.244-23C=
ENST00000647165.2:c.8089-23C= MANE Select	ENSP00000495481.1:n.8089-23C=
ENST00000651214.1:n.235-23C=
ENST00000205890.9:c.8089-23C=	ENSP00000205890.5:n.8089-23C=
ENST00000418233.7:c.-120-23C=	ENSP00000408800.3:n.-120-23C=
ENST00000445289.6:n.55C=
ENST00000536811.5:n.55C=
ENST00000585180.1:c.-143C=	ENSP00000464462.1:n.-143C=
ENST00000615845.4:c.8089-23C=	ENSP00000481642.1:n.8089-23C=
NM_016239.3:c.8089-23C=	NP_057323.3:n.8089-23C=
XM_011523921.1:c.8083-23C=	XP_011522223.1:n.8083-23C=
XM_017024714.2:c.8029-23C=	XP_016880203.1:n.8029-23C=
XM_017024715.2:c.8092-23C=	XP_016880204.1:n.8092-23C=
XR_001752809.1:n.297+32G=
XR_001752810.1:n.297+32G=
NM_016239.4:c.8089-23C= MANE Select	NP_057323.3:n.8089-23C=