Canonical Allele Identifier: CA1897925540
Gene: MYO3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26212150T= , CM000672.2:g.26212150T= GRCh38
NC_000010.10:g.26501079T= , CM000672.1:g.26501079T= GRCh37
NC_000010.9:g.26541085T= NCBI36
NG_011635.1:g.283078T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642920.2:c.*187T= MANE Select ENSP00000495965.1:n.*187T=
ENST00000644253.1:n.704T=
ENST00000645292.1:n.498T=
ENST00000647478.1:c.*1849T= ENSP00000493932.1:n.*1849T=
ENST00000265944.9:c.*187T= ENSP00000265944.4:n.*187T=
ENST00000543632.5:c.*89T= ENSP00000445909.1:n.*89T=
NM_017433.4:c.*187T= NP_059129.3:n.*187T=
XM_011519498.1:c.*187T= XP_011517800.1:n.*187T=
XM_011519499.1:c.*187T= XP_011517801.1:n.*187T=
XM_011519500.1:c.*187T= XP_011517802.1:n.*187T=
XM_011519501.1:c.*187T= XP_011517803.1:n.*187T=
XM_011519504.1:c.*89T= XP_011517806.1:n.*89T=
XM_011519505.1:c.*187T= XP_011517807.1:n.*187T=
XM_011519507.1:c.*187T= XP_011517809.1:n.*187T=
XM_011519512.1:c.*187T= XP_011517814.1:n.*187T=
XM_011519513.1:c.*187T= XP_011517815.1:n.*187T=
XR_930493.1:n.5135T=
XM_011519498.2:c.*187T= XP_011517800.1:n.*187T=
XM_011519500.2:c.*187T= XP_011517802.1:n.*187T=
XM_011519513.2:c.*187T= XP_011517815.1:n.*187T=
XR_001747111.1:n.4095T=
NM_017433.5:c.*187T= MANE Select NP_059129.3:n.*187T=