Canonical Allele Identifier: CA981989457

Gene: MYO15A

Linked Data

• dbSNP Id: rs2046557565
• gnomAD v3: 17-18150347-A-G
• gnomAD v4: 17-18150347-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150347A>G , CM000679.2:g.18150347A>G	GRCh38
NC_000017.10:g.18053661A>G , CM000679.1:g.18053661A>G	GRCh37
NC_000017.9:g.17994386A>G	NCBI36
NG_011634.1:g.46642A>G
NG_011634.2:g.46642A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7213-82A>G MANE Select	ENSP00000495481.1:n.7213-82A>G
ENST00000205890.9:c.7213-82A>G	ENSP00000205890.5:n.7213-82A>G
ENST00000615845.4:c.7213-82A>G	ENSP00000481642.1:n.7213-82A>G
NM_016239.3:c.7213-82A>G	NP_057323.3:n.7213-82A>G
XM_011523917.1:c.6888-82A>G	XP_011522219.1:n.6888-82A>G
XM_011523921.1:c.7207-82A>G	XP_011522223.1:n.7207-82A>G
XR_934037.1:n.7547-82A>G
XR_934038.1:n.7499-82A>G
XR_934293.1:n.434+1256T>C
XR_934294.1:n.435-574T>C
XR_934295.1:n.253+1256T>C
XM_017024714.2:c.7153-82A>G	XP_016880203.1:n.7153-82A>G
XM_017024715.2:c.7216-82A>G	XP_016880204.1:n.7216-82A>G
XR_934293.2:n.377+1256T>C
XR_934294.2:n.378-574T>C
NM_016239.4:c.7213-82A>G MANE Select	NP_057323.3:n.7213-82A>G