Canonical Allele Identifier: CA338233630

Gene: ATP13A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986891A>T , CM000663.2:g.16986891A>T	GRCh38
NC_000001.10:g.17313386A>T , CM000663.1:g.17313386A>T	GRCh37
NC_000001.9:g.17185973A>T	NCBI36
NG_009054.1:g.30038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3149T>A MANE Select	ENSP00000327214.8:p.Val1050Asp
ENST00000326735.12:c.3149T>A	ENSP00000327214.8:p.Val1050Asp
ENST00000341676.9:c.3017T>A	ENSP00000341115.5:p.Val1006Asp
ENST00000452699.5:c.3134T>A	ENSP00000413307.1:p.Val1045Asp
ENST00000466561.1:n.1023T>A
ENST00000502418.1:c.737T>A	ENSP00000423065.1:p.Val246Asp
NM_001141973.2:c.3134T>A	NP_001135445.1:p.Val1045Asp
NM_001141974.2:c.3017T>A	NP_001135446.1:p.Val1006Asp
NM_022089.3:c.3149T>A	NP_071372.1:p.Val1050Asp
XM_005245809.1:c.3149T>A	XP_005245866.1:p.Val1050Asp
XM_005245810.1:c.3146T>A	XP_005245867.1:p.Val1049Asp
XM_005245811.1:c.3134T>A	XP_005245868.1:p.Val1045Asp
XM_005245812.1:c.3122T>A	XP_005245869.1:p.Val1041Asp
XM_005245813.1:c.3089T>A	XP_005245870.1:p.Val1030Asp
XM_005245815.1:c.3032T>A	XP_005245872.1:p.Val1011Asp
XM_006710512.1:c.3131T>A	XP_006710575.1:p.Val1044Asp
XM_006710513.1:c.3107T>A	XP_006710576.1:p.Val1036Asp
XM_011541128.1:c.3134T>A	XP_011539430.1:p.Val1045Asp
XM_011541129.1:c.2942T>A	XP_011539431.1:p.Val981Asp
XM_017000844.1:c.3134T>A	XP_016856333.1:p.Val1045Asp
XM_017000845.1:c.3131T>A	XP_016856334.1:p.Val1044Asp
XM_017000846.1:c.3107T>A	XP_016856335.1:p.Val1036Asp
XM_017000847.1:c.3104T>A	XP_016856336.1:p.Val1035Asp
XM_017000848.1:c.3032T>A	XP_016856337.1:p.Val1011Asp
XM_017000849.1:c.3017T>A	XP_016856338.1:p.Val1006Asp
XM_017000850.1:c.2942T>A	XP_016856339.1:p.Val981Asp
NM_022089.4:c.3149T>A MANE Select	NP_071372.1:p.Val1050Asp
NM_001141973.3:c.3134T>A	NP_001135445.1:p.Val1045Asp
NM_001141974.3:c.3017T>A	NP_001135446.1:p.Val1006Asp