Canonical Allele Identifier: CA2697559456

Gene: MYO15A

Linked Data

• ClinVar Variation Id: 2757830
• ClinVar RCV Id: RCV003569400

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18124474C>G , CM000679.2:g.18124474C>G	GRCh38
NC_000017.10:g.18027788C>G , CM000679.1:g.18027788C>G	GRCh37
NC_000017.9:g.17968513C>G	NCBI36
NG_011634.1:g.20769C>G
NG_011634.2:g.20769C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.3610-9C>G MANE Select	ENSP00000495481.1:n.3610-9C>G
ENST00000651088.1:c.151-9C>G	ENSP00000498988.1:n.151-9C>G
ENST00000205890.9:c.3610-9C>G	ENSP00000205890.5:n.3610-9C>G
ENST00000583079.1:n.5307C>G
ENST00000615845.4:c.3610-9C>G	ENSP00000481642.1:n.3610-9C>G
NM_016239.3:c.3610-9C>G	NP_057323.3:n.3610-9C>G
XM_011523917.1:c.3610-9C>G	XP_011522219.1:n.3610-9C>G
XM_011523918.1:c.3610-9C>G	XP_011522220.1:n.3610-9C>G
XM_011523919.1:c.3610-9C>G	XP_011522221.1:n.3610-9C>G
XM_011523920.1:c.3610-9C>G	XP_011522222.1:n.3610-9C>G
XM_011523921.1:c.3610-9C>G	XP_011522223.1:n.3610-9C>G
XR_934037.1:n.4269-9C>G
XR_934038.1:n.4269-9C>G
XR_934039.1:n.4269-9C>G
XM_011523918.2:c.3610-9C>G	XP_011522220.1:n.3610-9C>G
XM_017024714.2:c.3610-9C>G	XP_016880203.1:n.3610-9C>G
XM_017024715.2:c.3610-9C>G	XP_016880204.1:n.3610-9C>G
XM_024450780.1:c.3610-9C>G	XP_024306548.1:n.3610-9C>G
XM_024450781.1:c.3610-9C>G	XP_024306549.1:n.3610-9C>G
XM_024450782.1:c.3610-9C>G	XP_024306550.1:n.3610-9C>G
XR_934039.2:n.4308-9C>G
NM_016239.4:c.3610-9C>G MANE Select	NP_057323.3:n.3610-9C>G