Canonical Allele Identifier: CA8425597

Gene: MYO15A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1836G>A
ENST00000643693.1:n.1374G>A
ENST00000644795.1:c.1364G>A	ENSP00000495720.1:p.Arg455His
ENST00000646782.1:n.2306G>A
ENST00000647165.2:c.9572G>A MANE Select	ENSP00000495481.1:p.Arg3191His
ENST00000651214.1:n.2003G>A
ENST00000205890.9:c.9572G>A	ENSP00000205890.5:p.Arg3191His
ENST00000418233.7:c.1364G>A	ENSP00000408800.3:p.Arg455His
ENST00000433411.7:n.1022G>A
ENST00000445289.6:n.502G>A
ENST00000473013.1:n.756G>A
ENST00000556535.5:c.434G>A	ENSP00000451782.1:p.Arg145His
ENST00000557190.5:n.400G>A
ENST00000557655.5:c.*252G>A	ENSP00000451925.1:n.*252G>A
ENST00000578575.1:c.135G>A
ENST00000579848.6:c.287G>A	ENSP00000465910.1:p.Arg96His
ENST00000615845.4:c.9572G>A	ENSP00000481642.1:p.Arg3191His
NM_016239.3:c.9572G>A	NP_057323.3:p.Arg3191His
XM_011523921.1:c.9566G>A	XP_011522223.1:p.Arg3189His
XM_017024714.2:c.9512G>A	XP_016880203.1:p.Arg3171His
XM_017024715.2:c.9575G>A	XP_016880204.1:p.Arg3192His
NM_016239.4:c.9572G>A MANE Select	NP_057323.3:p.Arg3191His