Canonical Allele Identifier: CA636878

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16990213C>T , CM000663.2:g.16990213C>T	GRCh38
NC_000001.10:g.17316708C>T , CM000663.1:g.17316708C>T	GRCh37
NC_000001.9:g.17189295C>T	NCBI36
NG_009054.1:g.26716G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022089.4:c.2326G>A MANE Select	NP_071372.1:p.Val776Ile
ENST00000326735.13:c.2326G>A MANE Select	ENSP00000327214.8:p.Val776Ile
NM_001141973.2:c.2311G>A	NP_001135445.1:p.Val771Ile
NM_001141973.3:c.2311G>A	NP_001135445.1:p.Val771Ile
NM_001141974.2:c.2311G>A	NP_001135446.1:p.Val771Ile
NM_001141974.3:c.2311G>A	NP_001135446.1:p.Val771Ile
NM_022089.3:c.2326G>A	NP_071372.1:p.Val776Ile
ENST00000326735.12:c.2326G>A	ENSP00000327214.8:p.Val776Ile
ENST00000341676.9:c.2311G>A	ENSP00000341115.5:p.Val771Ile
ENST00000452699.5:c.2311G>A	ENSP00000413307.1:p.Val771Ile
ENST00000466561.1:n.200G>A
ENST00000503552.1:c.736G>A	ENSP00000421126.1:p.Val246Ile
XM_005245809.1:c.2326G>A	XP_005245866.1:p.Val776Ile
XM_005245810.1:c.2323G>A	XP_005245867.1:p.Val775Ile
XM_005245811.1:c.2311G>A	XP_005245868.1:p.Val771Ile
XM_005245812.1:c.2299G>A	XP_005245869.1:p.Val767Ile
XM_005245813.1:c.2266G>A	XP_005245870.1:p.Val756Ile
XM_005245815.1:c.2326G>A	XP_005245872.1:p.Val776Ile
XM_006710512.1:c.2308G>A	XP_006710575.1:p.Val770Ile
XM_006710513.1:c.2284G>A	XP_006710576.1:p.Val762Ile
XM_011541128.1:c.2311G>A	XP_011539430.1:p.Val771Ile
XM_011541129.1:c.2119G>A	XP_011539431.1:p.Val707Ile
XM_017000844.1:c.2311G>A	XP_016856333.1:p.Val771Ile
XM_017000845.1:c.2308G>A	XP_016856334.1:p.Val770Ile
XM_017000846.1:c.2284G>A	XP_016856335.1:p.Val762Ile
XM_017000847.1:c.2281G>A	XP_016856336.1:p.Val761Ile
XM_017000848.1:c.2326G>A	XP_016856337.1:p.Val776Ile
XM_017000849.1:c.2311G>A	XP_016856338.1:p.Val771Ile
XM_017000850.1:c.2119G>A	XP_016856339.1:p.Val707Ile