Canonical Allele Identifier: CA2759937481

Gene: ATP13A4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467496A>G , CM000665.2:g.193467496A>G	GRCh38
NC_000003.11:g.193185285A>G , CM000665.1:g.193185285A>G	GRCh37
NC_000003.10:g.194667979A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.944-10T>C MANE Select	ENSP00000339182.4:n.944-10T>C
ENST00000295548.3:c.944-10T>C	ENSP00000295548.3:n.944-10T>C
ENST00000342695.8:c.944-10T>C	ENSP00000339182.4:n.944-10T>C
ENST00000392443.7:c.944-10T>C	ENSP00000376238.3:n.944-10T>C
ENST00000450950.6:c.*387-10T>C	ENSP00000402023.2:n.*387-10T>C
ENST00000490925.5:n.1052-10T>C
NM_032279.3:c.944-10T>C	NP_115655.2:n.944-10T>C
XM_005247829.2:c.944-10T>C	XP_005247886.1:n.944-10T>C
XM_011513232.1:c.944-10T>C	XP_011511534.1:n.944-10T>C
XR_241512.2:n.1245-10T>C
XR_924191.1:n.1245-10T>C
XM_011513232.2:c.944-10T>C	XP_011511534.1:n.944-10T>C
XM_017007318.1:c.617-10T>C	XP_016862807.1:n.617-10T>C
XM_017007319.1:c.944-10T>C	XP_016862808.1:n.944-10T>C
XR_001740324.2:n.1014-10T>C
XR_001740325.1:n.1014-10T>C
XR_002959602.1:n.1178-10T>C
XR_924191.3:n.1014-10T>C
NM_032279.4:c.944-10T>C MANE Select	NP_115655.2:n.944-10T>C