Canonical Allele Identifier: CA355784009

Gene: ATP13A4

Linked Data

• MyVariant Identifiers: chr3:g.193185232A>T (hg19) ; chr3:g.193467443A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467443A>T , CM000665.2:g.193467443A>T	GRCh38
NC_000003.11:g.193185232A>T , CM000665.1:g.193185232A>T	GRCh37
NC_000003.10:g.194667926A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.987T>A MANE Select	ENSP00000339182.4:p.Asp329Glu
ENST00000295548.3:c.987T>A	ENSP00000295548.3:p.Asp329Glu
ENST00000342695.8:c.987T>A	ENSP00000339182.4:p.Asp329Glu
ENST00000392443.7:c.987T>A	ENSP00000376238.3:p.Asp329Glu
ENST00000450950.6:c.*430T>A	ENSP00000402023.2:n.*430T>A
ENST00000490925.5:n.1095T>A
NM_032279.3:c.987T>A	NP_115655.2:p.Asp329Glu
XM_005247829.2:c.987T>A	XP_005247886.1:p.Asp329Glu
XM_011513232.1:c.987T>A	XP_011511534.1:p.Asp329Glu
XR_241512.2:n.1288T>A
XR_924191.1:n.1288T>A
XM_011513232.2:c.987T>A	XP_011511534.1:p.Asp329Glu
XM_017007318.1:c.660T>A	XP_016862807.1:p.Asp220Glu
XM_017007319.1:c.987T>A	XP_016862808.1:p.Asp329Glu
XR_001740324.2:n.1057T>A
XR_001740325.1:n.1057T>A
XR_002959602.1:n.1221T>A
XR_924191.3:n.1057T>A
NM_032279.4:c.987T>A MANE Select	NP_115655.2:p.Asp329Glu