Canonical Allele Identifier: CA398633796

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062612C>G (hg19) ; chr17:g.18159298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159298C>G , CM000679.2:g.18159298C>G	GRCh38
NC_000017.10:g.18062612C>G , CM000679.1:g.18062612C>G	GRCh37
NC_000017.9:g.18003337C>G	NCBI36
NG_011634.1:g.55593C>G
NG_011634.2:g.55593C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1518C>G
ENST00000643693.1:n.982C>G
ENST00000644795.1:c.972C>G	ENSP00000495720.1:p.Ile324Met
ENST00000646782.1:n.1914C>G
ENST00000647165.2:c.9180C>G MANE Select	ENSP00000495481.1:p.Ile3060Met
ENST00000651214.1:n.1685C>G
ENST00000205890.9:c.9180C>G	ENSP00000205890.5:p.Ile3060Met
ENST00000418233.7:c.972C>G	ENSP00000408800.3:p.Ile324Met
ENST00000433411.7:n.117C>G
ENST00000445289.6:n.316+1398C>G
ENST00000556535.5:c.42C>G	ENSP00000451782.1:p.Ile14Met
ENST00000557190.5:n.82C>G
ENST00000557655.5:c.42C>G	ENSP00000451925.1:p.Ile14Met
ENST00000578472.5:c.42C>G	ENSP00000467989.1:p.Ile14Met
ENST00000615845.4:c.9180C>G	ENSP00000481642.1:p.Ile3060Met
NM_016239.3:c.9180C>G	NP_057323.3:p.Ile3060Met
XM_011523921.1:c.9174C>G	XP_011522223.1:p.Ile3058Met
XM_017024714.2:c.9120C>G	XP_016880203.1:p.Ile3040Met
XM_017024715.2:c.9183C>G	XP_016880204.1:p.Ile3061Met
NM_016239.4:c.9180C>G MANE Select	NP_057323.3:p.Ile3060Met