Canonical Allele Identifier: CA2669096110

Gene: ATP13A4

Linked Data

• gnomAD v4: 3-193448380-C-CTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193448387_193448389dup , CM000665.2:g.193448387_193448389dup	GRCh38
NC_000003.11:g.193166176_193166178dup , CM000665.1:g.193166176_193166178dup	GRCh37
NC_000003.10:g.194648870_194648872dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.2028-53_2028-51dup MANE Select	ENSP00000339182.4:n.2028-53_2028-51dup
ENST00000342695.8:c.2028-53_2028-51dup	ENSP00000339182.4:n.2028-53_2028-51dup
ENST00000392443.7:c.1971-53_1971-51dup	ENSP00000376238.3:n.1971-53_1971-51dup
ENST00000428352.5:c.947-53_947-51dup
ENST00000450950.6:c.*1471-53_*1471-51dup	ENSP00000402023.2:n.*1471-53_*1471-51dup
ENST00000490925.5:n.2136-53_2136-51dup
NM_032279.3:c.2028-53_2028-51dup	NP_115655.2:n.2028-53_2028-51dup
XM_005247829.2:c.2028-53_2028-51dup	XP_005247886.1:n.2028-53_2028-51dup
XM_011513232.1:c.2028-53_2028-51dup	XP_011511534.1:n.2028-53_2028-51dup
XR_241512.2:n.2329-53_2329-51dup
XR_924191.1:n.2329-53_2329-51dup
XM_011513232.2:c.2028-53_2028-51dup	XP_011511534.1:n.2028-53_2028-51dup
XM_017007318.1:c.1701-53_1701-51dup	XP_016862807.1:n.1701-53_1701-51dup
XM_017007319.1:c.2028-53_2028-51dup	XP_016862808.1:n.2028-53_2028-51dup
XR_001740324.2:n.2098-53_2098-51dup
XR_001740325.1:n.2098-53_2098-51dup
XR_002959602.1:n.2262-53_2262-51dup
XR_924191.3:n.2098-53_2098-51dup
NM_032279.4:c.2028-53_2028-51dup MANE Select	NP_115655.2:n.2028-53_2028-51dup