Canonical Allele Identifier: CA625315113

Gene: MYO15A

Linked Data

• dbSNP Id: rs1333010220
• gnomAD v2: 17-18052781-T-G
• gnomAD v4: 17-18149467-T-G
• MyVariant Identifiers: chr17:g.18052781T>G (hg19) ; chr17:g.18149467T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149467T>G , CM000679.2:g.18149467T>G	GRCh38
NC_000017.10:g.18052781T>G , CM000679.1:g.18052781T>G	GRCh37
NC_000017.9:g.17993506T>G	NCBI36
NG_011634.1:g.45762T>G
NG_011634.2:g.45762T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7118-19T>G MANE Select	ENSP00000495481.1:n.7118-19T>G
ENST00000205890.9:c.7118-19T>G	ENSP00000205890.5:n.7118-19T>G
ENST00000578999.1:n.720T>G
ENST00000615845.4:c.7118-19T>G	ENSP00000481642.1:n.7118-19T>G
NM_016239.3:c.7118-19T>G	NP_057323.3:n.7118-19T>G
XM_011523917.1:c.6793-19T>G	XP_011522219.1:n.6793-19T>G
XM_011523921.1:c.7112-19T>G	XP_011522223.1:n.7112-19T>G
XR_934037.1:n.7452-19T>G
XR_934038.1:n.7404-19T>G
XR_934293.1:n.435-1861A>C
XR_934295.1:n.254-1861A>C
XM_017024714.2:c.7058-19T>G	XP_016880203.1:n.7058-19T>G
XM_017024715.2:c.7121-19T>G	XP_016880204.1:n.7121-19T>G
XR_934293.2:n.378-1861A>C
NM_016239.4:c.7118-19T>G MANE Select	NP_057323.3:n.7118-19T>G