Canonical Allele Identifier: CA1430177730
Gene: ATP13A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193448393A= , CM000665.2:g.193448393A= GRCh38
NC_000003.11:g.193166182A= , CM000665.1:g.193166182A= GRCh37
NC_000003.10:g.194648876A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342695.9:c.2028-63T= MANE Select ENSP00000339182.4:n.2028-63T=
ENST00000342695.8:c.2028-63T= ENSP00000339182.4:n.2028-63T=
ENST00000392443.7:c.1971-63T= ENSP00000376238.3:n.1971-63T=
ENST00000428352.5:c.947-63T=
ENST00000450950.6:c.*1471-63T= ENSP00000402023.2:n.*1471-63T=
ENST00000490925.5:n.2136-63T=
NM_032279.3:c.2028-63T= NP_115655.2:n.2028-63T=
XM_005247829.2:c.2028-63T= XP_005247886.1:n.2028-63T=
XM_011513232.1:c.2028-63T= XP_011511534.1:n.2028-63T=
XR_241512.2:n.2329-63T=
XR_924191.1:n.2329-63T=
XM_011513232.2:c.2028-63T= XP_011511534.1:n.2028-63T=
XM_017007318.1:c.1701-63T= XP_016862807.1:n.1701-63T=
XM_017007319.1:c.2028-63T= XP_016862808.1:n.2028-63T=
XR_001740324.2:n.2098-63T=
XR_001740325.1:n.2098-63T=
XR_002959602.1:n.2262-63T=
XR_924191.3:n.2098-63T=
NM_032279.4:c.2028-63T= MANE Select NP_115655.2:n.2028-63T=