Canonical Allele Identifier: CA2250881595

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18162639G= , CM000679.2:g.18162639G=	GRCh38
NC_000017.10:g.18065953G= , CM000679.1:g.18065953G=	GRCh37
NC_000017.9:g.18006678G=	NCBI36
NG_011634.1:g.58934G=
NG_011634.2:g.58934G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1836G=
ENST00000643693.1:n.1374G=
ENST00000644795.1:c.1364G=	ENSP00000495720.1:p.Arg455=
ENST00000646782.1:n.2306G=
ENST00000647165.2:c.9572G= MANE Select	ENSP00000495481.1:p.Arg3191=
ENST00000651214.1:n.2003G=
ENST00000205890.9:c.9572G=	ENSP00000205890.5:p.Arg3191=
ENST00000418233.7:c.1364G=	ENSP00000408800.3:p.Arg455=
ENST00000433411.7:n.1022G=
ENST00000445289.6:n.502G=
ENST00000473013.1:n.756G=
ENST00000556535.5:c.434G=	ENSP00000451782.1:p.Arg145=
ENST00000557190.5:n.400G=
ENST00000557655.5:c.*252G=	ENSP00000451925.1:n.*252G=
ENST00000578575.1:c.135G=
ENST00000579848.6:c.287G=	ENSP00000465910.1:p.Arg96=
ENST00000615845.4:c.9572G=	ENSP00000481642.1:p.Arg3191=
NM_016239.3:c.9572G=	NP_057323.3:p.Arg3191=
XM_011523921.1:c.9566G=	XP_011522223.1:p.Arg3189=
XM_017024714.2:c.9512G=	XP_016880203.1:p.Arg3171=
XM_017024715.2:c.9575G=	XP_016880204.1:p.Arg3192=
NM_016239.4:c.9572G= MANE Select	NP_057323.3:p.Arg3191=