Canonical Allele Identifier: CA498203911

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18159292-C-A
• MyVariant Identifiers: chr17:g.18062606C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159292C>A , CM000679.2:g.18159292C>A	GRCh38
NC_000017.10:g.18062606C>A , CM000679.1:g.18062606C>A	GRCh37
NC_000017.9:g.18003331C>A	NCBI36
NG_011634.1:g.55587C>A
NG_011634.2:g.55587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1512C>A
ENST00000643693.1:n.976C>A
ENST00000644795.1:c.966C>A	ENSP00000495720.1:p.Ser322=
ENST00000646782.1:n.1908C>A
ENST00000647165.2:c.9174C>A MANE Select	ENSP00000495481.1:p.Ser3058=
ENST00000651214.1:n.1679C>A
ENST00000205890.9:c.9174C>A	ENSP00000205890.5:p.Ser3058=
ENST00000418233.7:c.966C>A	ENSP00000408800.3:p.Ser322=
ENST00000433411.7:n.111C>A
ENST00000445289.6:n.316+1392C>A
ENST00000556535.5:c.36C>A	ENSP00000451782.1:p.Ser12=
ENST00000557190.5:n.76C>A
ENST00000557655.5:c.36C>A	ENSP00000451925.1:p.Ser12=
ENST00000578472.5:c.36C>A	ENSP00000467989.1:p.Ser12=
ENST00000615845.4:c.9174C>A	ENSP00000481642.1:p.Ser3058=
NM_016239.3:c.9174C>A	NP_057323.3:p.Ser3058=
XM_011523921.1:c.9168C>A	XP_011522223.1:p.Ser3056=
XM_017024714.2:c.9114C>A	XP_016880203.1:p.Ser3038=
XM_017024715.2:c.9177C>A	XP_016880204.1:p.Ser3059=
NM_016239.4:c.9174C>A MANE Select	NP_057323.3:p.Ser3058=