Canonical Allele Identifier: CA2830536197

Gene: ATP13A4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467501del , CM000665.2:g.193467501del	GRCh38
NC_000003.11:g.193185290del , CM000665.1:g.193185290del	GRCh37
NC_000003.10:g.194667984del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.944-15del MANE Select	ENSP00000339182.4:n.944-15del
ENST00000295548.3:c.944-15del	ENSP00000295548.3:n.944-15del
ENST00000342695.8:c.944-15del	ENSP00000339182.4:n.944-15del
ENST00000392443.7:c.944-15del	ENSP00000376238.3:n.944-15del
ENST00000450950.6:c.*387-15del	ENSP00000402023.2:n.*387-15del
ENST00000490925.5:n.1052-15del
NM_032279.3:c.944-15del	NP_115655.2:n.944-15del
XM_005247829.2:c.944-15del	XP_005247886.1:n.944-15del
XM_011513232.1:c.944-15del	XP_011511534.1:n.944-15del
XR_241512.2:n.1245-15del
XR_924191.1:n.1245-15del
XM_011513232.2:c.944-15del	XP_011511534.1:n.944-15del
XM_017007318.1:c.617-15del	XP_016862807.1:n.617-15del
XM_017007319.1:c.944-15del	XP_016862808.1:n.944-15del
XR_001740324.2:n.1014-15del
XR_001740325.1:n.1014-15del
XR_002959602.1:n.1178-15del
XR_924191.3:n.1014-15del
NM_032279.4:c.944-15del MANE Select	NP_115655.2:n.944-15del