Canonical Allele Identifier: CA398633939

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062630C>A (hg19) ; chr17:g.18159316C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159316C>A , CM000679.2:g.18159316C>A	GRCh38
NC_000017.10:g.18062630C>A , CM000679.1:g.18062630C>A	GRCh37
NC_000017.9:g.18003355C>A	NCBI36
NG_011634.1:g.55611C>A
NG_011634.2:g.55611C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1536C>A
ENST00000643693.1:n.1000C>A
ENST00000644795.1:c.990C>A	ENSP00000495720.1:p.Ser330Arg
ENST00000646782.1:n.1932C>A
ENST00000647165.2:c.9198C>A MANE Select	ENSP00000495481.1:p.Ser3066Arg
ENST00000651214.1:n.1703C>A
ENST00000205890.9:c.9198C>A	ENSP00000205890.5:p.Ser3066Arg
ENST00000418233.7:c.990C>A	ENSP00000408800.3:p.Ser330Arg
ENST00000433411.7:n.135C>A
ENST00000445289.6:n.316+1416C>A
ENST00000556535.5:c.60C>A	ENSP00000451782.1:p.Ser20Arg
ENST00000557190.5:n.100C>A
ENST00000557655.5:c.60C>A	ENSP00000451925.1:p.Ser20Arg
ENST00000578472.5:c.60C>A	ENSP00000467989.1:p.Ser20Arg
ENST00000615845.4:c.9198C>A	ENSP00000481642.1:p.Ser3066Arg
NM_016239.3:c.9198C>A	NP_057323.3:p.Ser3066Arg
XM_011523921.1:c.9192C>A	XP_011522223.1:p.Ser3064Arg
XM_017024714.2:c.9138C>A	XP_016880203.1:p.Ser3046Arg
XM_017024715.2:c.9201C>A	XP_016880204.1:p.Ser3067Arg
NM_016239.4:c.9198C>A MANE Select	NP_057323.3:p.Ser3066Arg