Canonical Allele Identifier: CA398633822

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18159302-C-G
• MyVariant Identifiers: chr17:g.18062616C>G (hg19) ; chr17:g.18159302C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159302C>G , CM000679.2:g.18159302C>G	GRCh38
NC_000017.10:g.18062616C>G , CM000679.1:g.18062616C>G	GRCh37
NC_000017.9:g.18003341C>G	NCBI36
NG_011634.1:g.55597C>G
NG_011634.2:g.55597C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1522C>G
ENST00000643693.1:n.986C>G
ENST00000644795.1:c.976C>G	ENSP00000495720.1:p.Leu326Val
ENST00000646782.1:n.1918C>G
ENST00000647165.2:c.9184C>G MANE Select	ENSP00000495481.1:p.Leu3062Val
ENST00000651214.1:n.1689C>G
ENST00000205890.9:c.9184C>G	ENSP00000205890.5:p.Leu3062Val
ENST00000418233.7:c.976C>G	ENSP00000408800.3:p.Leu326Val
ENST00000433411.7:n.121C>G
ENST00000445289.6:n.316+1402C>G
ENST00000556535.5:c.46C>G	ENSP00000451782.1:p.Leu16Val
ENST00000557190.5:n.86C>G
ENST00000557655.5:c.46C>G	ENSP00000451925.1:p.Leu16Val
ENST00000578472.5:c.46C>G	ENSP00000467989.1:p.Leu16Val
ENST00000615845.4:c.9184C>G	ENSP00000481642.1:p.Leu3062Val
NM_016239.3:c.9184C>G	NP_057323.3:p.Leu3062Val
XM_011523921.1:c.9178C>G	XP_011522223.1:p.Leu3060Val
XM_017024714.2:c.9124C>G	XP_016880203.1:p.Leu3042Val
XM_017024715.2:c.9187C>G	XP_016880204.1:p.Leu3063Val
NM_016239.4:c.9184C>G MANE Select	NP_057323.3:p.Leu3062Val