Canonical Allele Identifier: CA393053606
Community Standard Title: NM_006901.4(MYO9A):c.1658G>A (p.Cys553Tyr)
Gene: MYO9A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.71991167C>T , CM000677.2:g.71991167C>T GRCh38
NC_000015.9:g.72283508C>T , CM000677.1:g.72283508C>T GRCh37
NC_000015.8:g.70070562C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006901.4:c.1658G>A MANE Select NP_008832.2:p.Cys553Tyr
ENST00000356056.10:c.1658G>A MANE Select ENSP00000348349.5:p.Cys553Tyr
NM_006901.3:c.1658G>A NP_008832.2:p.Cys553Tyr
ENST00000356056.9:c.1658G>A ENSP00000348349.5:p.Cys553Tyr
ENST00000424560.2:c.1658G>A ENSP00000399162.2:p.Cys553Tyr
ENST00000444904.5:c.1658G>A ENSP00000398250.2:p.Cys553Tyr
ENST00000563542.5:n.1674G>A
ENST00000564571.5:c.1658G>A ENSP00000456192.1:p.Cys553Tyr
ENST00000566885.5:c.443G>A ENSP00000454446.1:p.Cys148Tyr
ENST00000567560.5:n.2131G>A
XM_006720539.1:c.1658G>A XP_006720602.1:p.Cys553Tyr
XM_006720539.3:c.1658G>A XP_006720602.1:p.Cys553Tyr
XM_011521613.1:c.1658G>A XP_011519915.1:p.Cys553Tyr
XM_011521613.3:c.1658G>A XP_011519915.1:p.Cys553Tyr
XM_011521614.1:c.1658G>A XP_011519916.1:p.Cys553Tyr
XM_011521614.3:c.1658G>A XP_011519916.1:p.Cys553Tyr
XM_011521615.1:c.1658G>A XP_011519917.1:p.Cys553Tyr
XM_011521615.3:c.1658G>A XP_011519917.1:p.Cys553Tyr
XM_011521616.1:c.1658G>A XP_011519918.1:p.Cys553Tyr
XM_011521616.3:c.1658G>A XP_011519918.1:p.Cys553Tyr
XM_011521617.1:c.1658G>A XP_011519919.1:p.Cys553Tyr
XM_011521617.3:c.1658G>A XP_011519919.1:p.Cys553Tyr
XM_011521618.1:c.1658G>A XP_011519920.1:p.Cys553Tyr
XM_011521618.3:c.1658G>A XP_011519920.1:p.Cys553Tyr
XM_011521619.1:c.1601G>A XP_011519921.1:p.Cys534Tyr
XM_011521619.3:c.1601G>A XP_011519921.1:p.Cys534Tyr
XM_011521620.1:c.1601G>A XP_011519922.1:p.Cys534Tyr
XM_011521620.3:c.1601G>A XP_011519922.1:p.Cys534Tyr
XM_011521621.1:c.1658G>A XP_011519923.1:p.Cys553Tyr
XM_011521621.3:c.1658G>A XP_011519923.1:p.Cys553Tyr
XM_011521622.1:c.1658G>A XP_011519924.1:p.Cys553Tyr
XM_011521622.3:c.1658G>A XP_011519924.1:p.Cys553Tyr
XM_017022229.1:c.1658G>A XP_016877718.1:p.Cys553Tyr
XM_017022230.2:c.1601G>A XP_016877719.1:p.Cys534Tyr