Canonical Allele Identifier: CA398638238

Gene: MYO15A

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1836G>T
ENST00000643693.1:n.1374G>T
ENST00000644795.1:c.1364G>T	ENSP00000495720.1:p.Arg455Leu
ENST00000646782.1:n.2306G>T
ENST00000647165.2:c.9572G>T MANE Select	ENSP00000495481.1:p.Arg3191Leu
ENST00000651214.1:n.2003G>T
ENST00000205890.9:c.9572G>T	ENSP00000205890.5:p.Arg3191Leu
ENST00000418233.7:c.1364G>T	ENSP00000408800.3:p.Arg455Leu
ENST00000433411.7:n.1022G>T
ENST00000445289.6:n.502G>T
ENST00000473013.1:n.756G>T
ENST00000556535.5:c.434G>T	ENSP00000451782.1:p.Arg145Leu
ENST00000557190.5:n.400G>T
ENST00000557655.5:c.*252G>T	ENSP00000451925.1:n.*252G>T
ENST00000578575.1:c.135G>T
ENST00000579848.6:c.287G>T	ENSP00000465910.1:p.Arg96Leu
ENST00000615845.4:c.9572G>T	ENSP00000481642.1:p.Arg3191Leu
NM_016239.3:c.9572G>T	NP_057323.3:p.Arg3191Leu
XM_011523921.1:c.9566G>T	XP_011522223.1:p.Arg3189Leu
XM_017024714.2:c.9512G>T	XP_016880203.1:p.Arg3171Leu
XM_017024715.2:c.9575G>T	XP_016880204.1:p.Arg3192Leu
NM_016239.4:c.9572G>T MANE Select	NP_057323.3:p.Arg3191Leu