Canonical Allele Identifier: CA437431030

Gene: ATP13A4

Linked Data

• dbSNP Id: rs369458872
• MyVariant Identifiers: chr3:g.193185247C>A (hg19) ; chr3:g.193467458C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467458C>A , CM000665.2:g.193467458C>A	GRCh38
NC_000003.11:g.193185247C>A , CM000665.1:g.193185247C>A	GRCh37
NC_000003.10:g.194667941C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.972G>T MANE Select	ENSP00000339182.4:p.Pro324=
ENST00000295548.3:c.972G>T	ENSP00000295548.3:p.Pro324=
ENST00000342695.8:c.972G>T	ENSP00000339182.4:p.Pro324=
ENST00000392443.7:c.972G>T	ENSP00000376238.3:p.Pro324=
ENST00000450950.6:c.*415G>T	ENSP00000402023.2:n.*415G>T
ENST00000490925.5:n.1080G>T
NM_032279.3:c.972G>T	NP_115655.2:p.Pro324=
XM_005247829.2:c.972G>T	XP_005247886.1:p.Pro324=
XM_011513232.1:c.972G>T	XP_011511534.1:p.Pro324=
XR_241512.2:n.1273G>T
XR_924191.1:n.1273G>T
XM_011513232.2:c.972G>T	XP_011511534.1:p.Pro324=
XM_017007318.1:c.645G>T	XP_016862807.1:p.Pro215=
XM_017007319.1:c.972G>T	XP_016862808.1:p.Pro324=
XR_001740324.2:n.1042G>T
XR_001740325.1:n.1042G>T
XR_002959602.1:n.1206G>T
XR_924191.3:n.1042G>T
NM_032279.4:c.972G>T MANE Select	NP_115655.2:p.Pro324=