Canonical Allele Identifier: CA1897925539

Gene: MYO3A

Linked Data

• dbSNP Id: rs1844249174
• gnomAD v4: 10-26212149-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212149C>G , CM000672.2:g.26212149C>G	GRCh38
NC_000010.10:g.26501078C>G , CM000672.1:g.26501078C>G	GRCh37
NC_000010.9:g.26541084C>G	NCBI36
NG_011635.1:g.283077C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642920.2:c.*186C>G MANE Select	ENSP00000495965.1:n.*186C>G
ENST00000644253.1:n.703C>G
ENST00000645292.1:n.497C>G
ENST00000647478.1:c.*1848C>G	ENSP00000493932.1:n.*1848C>G
ENST00000265944.9:c.*186C>G	ENSP00000265944.4:n.*186C>G
ENST00000543632.5:c.*88C>G	ENSP00000445909.1:n.*88C>G
NM_017433.4:c.*186C>G	NP_059129.3:n.*186C>G
XM_011519498.1:c.*186C>G	XP_011517800.1:n.*186C>G
XM_011519499.1:c.*186C>G	XP_011517801.1:n.*186C>G
XM_011519500.1:c.*186C>G	XP_011517802.1:n.*186C>G
XM_011519501.1:c.*186C>G	XP_011517803.1:n.*186C>G
XM_011519504.1:c.*88C>G	XP_011517806.1:n.*88C>G
XM_011519505.1:c.*186C>G	XP_011517807.1:n.*186C>G
XM_011519507.1:c.*186C>G	XP_011517809.1:n.*186C>G
XM_011519512.1:c.*186C>G	XP_011517814.1:n.*186C>G
XM_011519513.1:c.*186C>G	XP_011517815.1:n.*186C>G
XR_930493.1:n.5134C>G
XM_011519498.2:c.*186C>G	XP_011517800.1:n.*186C>G
XM_011519500.2:c.*186C>G	XP_011517802.1:n.*186C>G
XM_011519513.2:c.*186C>G	XP_011517815.1:n.*186C>G
XR_001747111.1:n.4094C>G
NM_017433.5:c.*186C>G MANE Select	NP_059129.3:n.*186C>G