Canonical Allele Identifier: CA288415784

Gene: MYO15A

Linked Data

• dbSNP Id: rs867898759
• gnomAD v4: 17-18159447-C-G
• MyVariant Identifiers: chr17:g.18062761C>G (hg19) ; chr17:g.18159447C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159447C>G , CM000679.2:g.18159447C>G	GRCh38
NC_000017.10:g.18062761C>G , CM000679.1:g.18062761C>G	GRCh37
NC_000017.9:g.18003486C>G	NCBI36
NG_011634.1:g.55742C>G
NG_011634.2:g.55742C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1567+100C>G
ENST00000643693.1:n.1031+100C>G
ENST00000644795.1:c.1021+100C>G	ENSP00000495720.1:n.1021+100C>G
ENST00000646782.1:n.1963+100C>G
ENST00000647165.2:c.9229+100C>G MANE Select	ENSP00000495481.1:n.9229+100C>G
ENST00000651214.1:n.1734+100C>G
ENST00000205890.9:c.9229+100C>G	ENSP00000205890.5:n.9229+100C>G
ENST00000418233.7:c.1021+100C>G	ENSP00000408800.3:n.1021+100C>G
ENST00000433411.7:n.266C>G
ENST00000445289.6:n.316+1547C>G
ENST00000556535.5:c.91+100C>G	ENSP00000451782.1:n.91+100C>G
ENST00000557190.5:n.131+100C>G
ENST00000557655.5:c.91+100C>G	ENSP00000451925.1:n.91+100C>G
ENST00000578472.5:c.91+100C>G	ENSP00000467989.1:n.91+100C>G
ENST00000615845.4:c.9229+100C>G	ENSP00000481642.1:n.9229+100C>G
NM_016239.3:c.9229+100C>G	NP_057323.3:n.9229+100C>G
XM_011523921.1:c.9223+100C>G	XP_011522223.1:n.9223+100C>G
XM_017024714.2:c.9169+100C>G	XP_016880203.1:n.9169+100C>G
XM_017024715.2:c.9232+100C>G	XP_016880204.1:n.9232+100C>G
NM_016239.4:c.9229+100C>G MANE Select	NP_057323.3:n.9229+100C>G