Canonical Allele Identifier: CA8425428

Gene: MYO15A

Linked Data

• ClinVar Variation Id: 3024012
• ClinVar RCV Id: RCV003881107
• dbSNP Id: rs540808631
• ExAC: 17:18062680 A / G
• gnomAD v2: 17-18062680-A-G
• gnomAD v3: 17-18159366-A-G
• gnomAD v4: 17-18159366-A-G
• MyVariant Identifiers: chr17:g.18062680A>G (hg19) ; chr17:g.18159366A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159366A>G , CM000679.2:g.18159366A>G	GRCh38
NC_000017.10:g.18062680A>G , CM000679.1:g.18062680A>G	GRCh37
NC_000017.9:g.18003405A>G	NCBI36
NG_011634.1:g.55661A>G
NG_011634.2:g.55661A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642418.1:n.1567+19A>G
ENST00000643693.1:n.1031+19A>G
ENST00000644795.1:c.1021+19A>G	ENSP00000495720.1:n.1021+19A>G
ENST00000646782.1:n.1963+19A>G
ENST00000647165.2:c.9229+19A>G MANE Select	ENSP00000495481.1:n.9229+19A>G
ENST00000651214.1:n.1734+19A>G
ENST00000205890.9:c.9229+19A>G	ENSP00000205890.5:n.9229+19A>G
ENST00000418233.7:c.1021+19A>G	ENSP00000408800.3:n.1021+19A>G
ENST00000433411.7:n.185A>G
ENST00000445289.6:n.316+1466A>G
ENST00000556535.5:c.91+19A>G	ENSP00000451782.1:n.91+19A>G
ENST00000557190.5:n.131+19A>G
ENST00000557655.5:c.91+19A>G	ENSP00000451925.1:n.91+19A>G
ENST00000578472.5:c.91+19A>G	ENSP00000467989.1:n.91+19A>G
ENST00000615845.4:c.9229+19A>G	ENSP00000481642.1:n.9229+19A>G
NM_016239.3:c.9229+19A>G	NP_057323.3:n.9229+19A>G
XM_011523921.1:c.9223+19A>G	XP_011522223.1:n.9223+19A>G
XM_017024714.2:c.9169+19A>G	XP_016880203.1:n.9169+19A>G
XM_017024715.2:c.9232+19A>G	XP_016880204.1:n.9232+19A>G
NM_016239.4:c.9229+19A>G MANE Select	NP_057323.3:n.9229+19A>G