Canonical Allele Identifier: CA1156031462

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16996396G= , CM000663.2:g.16996396G=	GRCh38
NC_000001.10:g.17322891G= , CM000663.1:g.17322891G=	GRCh37
NC_000001.9:g.17195478G=	NCBI36
NG_009054.1:g.20533C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1296C= MANE Select	ENSP00000327214.8:p.Leu432=
ENST00000326735.12:c.1296C=	ENSP00000327214.8:p.Leu432=
ENST00000341676.9:c.1281C=	ENSP00000341115.5:p.Leu427=
ENST00000452699.5:c.1281C=	ENSP00000413307.1:p.Leu427=
ENST00000463860.5:n.904C=
ENST00000502860.1:n.335-96C=
ENST00000506174.5:c.438C=	ENSP00000424393.1:p.Leu146=
ENST00000509392.1:n.299C=
ENST00000617114.4:c.335-96C=	ENSP00000478781.1:n.335-96C=
NM_001141973.2:c.1281C=	NP_001135445.1:p.Leu427=
NM_001141974.2:c.1281C=	NP_001135446.1:p.Leu427=
NM_022089.3:c.1296C=	NP_071372.1:p.Leu432=
XM_005245809.1:c.1296C=	XP_005245866.1:p.Leu432=
XM_005245810.1:c.1293C=	XP_005245867.1:p.Leu431=
XM_005245811.1:c.1281C=	XP_005245868.1:p.Leu427=
XM_005245812.1:c.1269C=	XP_005245869.1:p.Leu423=
XM_005245813.1:c.1296C=	XP_005245870.1:p.Leu432=
XM_005245815.1:c.1296C=	XP_005245872.1:p.Leu432=
XM_006710512.1:c.1278C=	XP_006710575.1:p.Leu426=
XM_006710513.1:c.1254C=	XP_006710576.1:p.Leu418=
XM_011541128.1:c.1296C=	XP_011539430.1:p.Leu432=
XM_011541129.1:c.1296C=	XP_011539431.1:p.Leu432=
XM_017000844.1:c.1296C=	XP_016856333.1:p.Leu432=
XM_017000845.1:c.1278C=	XP_016856334.1:p.Leu426=
XM_017000846.1:c.1254C=	XP_016856335.1:p.Leu418=
XM_017000847.1:c.1266C=	XP_016856336.1:p.Leu422=
XM_017000848.1:c.1296C=	XP_016856337.1:p.Leu432=
XM_017000849.1:c.1281C=	XP_016856338.1:p.Leu427=
XM_017000850.1:c.1296C=	XP_016856339.1:p.Leu432=
NM_022089.4:c.1296C= MANE Select	NP_071372.1:p.Leu432=
NM_001141973.3:c.1281C=	NP_001135445.1:p.Leu427=
NM_001141974.3:c.1281C=	NP_001135446.1:p.Leu427=