Canonical Allele Identifier: CA355783918
Gene: ATP13A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193467402T>A , CM000665.2:g.193467402T>A GRCh38
NC_000003.11:g.193185191T>A , CM000665.1:g.193185191T>A GRCh37
NC_000003.10:g.194667885T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342695.9:c.1028A>T MANE Select ENSP00000339182.4:p.Lys343Met
ENST00000295548.3:c.1028A>T ENSP00000295548.3:p.Lys343Met
ENST00000342695.8:c.1028A>T ENSP00000339182.4:p.Lys343Met
ENST00000392443.7:c.1028A>T ENSP00000376238.3:p.Lys343Met
ENST00000450950.6:c.*471A>T ENSP00000402023.2:n.*471A>T
ENST00000490925.5:n.1136A>T
NM_032279.3:c.1028A>T NP_115655.2:p.Lys343Met
XM_005247829.2:c.1028A>T XP_005247886.1:p.Lys343Met
XM_011513232.1:c.1028A>T XP_011511534.1:p.Lys343Met
XR_241512.2:n.1329A>T
XR_924191.1:n.1329A>T
XM_011513232.2:c.1028A>T XP_011511534.1:p.Lys343Met
XM_017007318.1:c.701A>T XP_016862807.1:p.Lys234Met
XM_017007319.1:c.1028A>T XP_016862808.1:p.Lys343Met
XR_001740324.2:n.1098A>T
XR_001740325.1:n.1098A>T
XR_002959602.1:n.1262A>T
XR_924191.3:n.1098A>T
NM_032279.4:c.1028A>T MANE Select NP_115655.2:p.Lys343Met