Canonical Allele Identifier: CA1897925527
Gene: MYO3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26212133C= , CM000672.2:g.26212133C= GRCh38
NC_000010.10:g.26501062C= , CM000672.1:g.26501062C= GRCh37
NC_000010.9:g.26541068C= NCBI36
NG_011635.1:g.283061C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642920.2:c.*170C= MANE Select ENSP00000495965.1:n.*170C=
ENST00000644253.1:n.687C=
ENST00000645292.1:n.481C=
ENST00000647478.1:c.*1832C= ENSP00000493932.1:n.*1832C=
ENST00000265944.9:c.*170C= ENSP00000265944.4:n.*170C=
ENST00000543632.5:c.*72C= ENSP00000445909.1:n.*72C=
NM_017433.4:c.*170C= NP_059129.3:n.*170C=
XM_011519498.1:c.*170C= XP_011517800.1:n.*170C=
XM_011519499.1:c.*170C= XP_011517801.1:n.*170C=
XM_011519500.1:c.*170C= XP_011517802.1:n.*170C=
XM_011519501.1:c.*170C= XP_011517803.1:n.*170C=
XM_011519504.1:c.*72C= XP_011517806.1:n.*72C=
XM_011519505.1:c.*170C= XP_011517807.1:n.*170C=
XM_011519507.1:c.*170C= XP_011517809.1:n.*170C=
XM_011519512.1:c.*170C= XP_011517814.1:n.*170C=
XM_011519513.1:c.*170C= XP_011517815.1:n.*170C=
XR_930493.1:n.5118C=
XM_011519498.2:c.*170C= XP_011517800.1:n.*170C=
XM_011519500.2:c.*170C= XP_011517802.1:n.*170C=
XM_011519513.2:c.*170C= XP_011517815.1:n.*170C=
XR_001747111.1:n.4078C=
NM_017433.5:c.*170C= MANE Select NP_059129.3:n.*170C=