Canonical Allele Identifier: CA398633913

Gene: MYO15A

Linked Data

• COSMIC: COSM976229
• MyVariant Identifiers: chr17:g.18062626G>T (hg19) ; chr17:g.18159312G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159312G>T , CM000679.2:g.18159312G>T	GRCh38
NC_000017.10:g.18062626G>T , CM000679.1:g.18062626G>T	GRCh37
NC_000017.9:g.18003351G>T	NCBI36
NG_011634.1:g.55607G>T
NG_011634.2:g.55607G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1532G>T
ENST00000643693.1:n.996G>T
ENST00000644795.1:c.986G>T	ENSP00000495720.1:p.Ser329Ile
ENST00000646782.1:n.1928G>T
ENST00000647165.2:c.9194G>T MANE Select	ENSP00000495481.1:p.Ser3065Ile
ENST00000651214.1:n.1699G>T
ENST00000205890.9:c.9194G>T	ENSP00000205890.5:p.Ser3065Ile
ENST00000418233.7:c.986G>T	ENSP00000408800.3:p.Ser329Ile
ENST00000433411.7:n.131G>T
ENST00000445289.6:n.316+1412G>T
ENST00000556535.5:c.56G>T	ENSP00000451782.1:p.Ser19Ile
ENST00000557190.5:n.96G>T
ENST00000557655.5:c.56G>T	ENSP00000451925.1:p.Ser19Ile
ENST00000578472.5:c.56G>T	ENSP00000467989.1:p.Ser19Ile
ENST00000615845.4:c.9194G>T	ENSP00000481642.1:p.Ser3065Ile
NM_016239.3:c.9194G>T	NP_057323.3:p.Ser3065Ile
XM_011523921.1:c.9188G>T	XP_011522223.1:p.Ser3063Ile
XM_017024714.2:c.9134G>T	XP_016880203.1:p.Ser3045Ile
XM_017024715.2:c.9197G>T	XP_016880204.1:p.Ser3066Ile
NM_016239.4:c.9194G>T MANE Select	NP_057323.3:p.Ser3065Ile