Canonical Allele Identifier: CA1156049306

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986240G= , CM000663.2:g.16986240G=	GRCh38
NC_000001.10:g.17312735G= , CM000663.1:g.17312735G=	GRCh37
NC_000001.9:g.17185322G=	NCBI36
NG_009054.1:g.30689C=
NG_029688.1:g.347C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.3524C= MANE Select	ENSP00000327214.8:p.Pro1175=
ENST00000326735.12:c.3524C=	ENSP00000327214.8:p.Pro1175=
ENST00000341676.9:c.3222C=	ENSP00000341115.5:p.Ala1074=
ENST00000452699.5:c.3509C=	ENSP00000413307.1:p.Pro1170=
ENST00000466561.1:n.1570C=
ENST00000502418.1:c.942C=	ENSP00000423065.1:p.Ala314=
NM_001141973.2:c.3509C=	NP_001135445.1:p.Pro1170=
NM_001141974.2:c.3222C=	NP_001135446.1:p.Ala1074=
NM_022089.3:c.3524C=	NP_071372.1:p.Pro1175=
XM_005245809.1:c.3354C=	XP_005245866.1:p.Ala1118=
XM_005245810.1:c.3351C=	XP_005245867.1:p.Ala1117=
XM_005245811.1:c.3339C=	XP_005245868.1:p.Ala1113=
XM_005245812.1:c.3327C=	XP_005245869.1:p.Ala1109=
XM_005245813.1:c.3294C=	XP_005245870.1:p.Ala1098=
XM_005245815.1:c.3237C=	XP_005245872.1:p.Ala1079=
XM_006710512.1:c.3336C=	XP_006710575.1:p.Ala1112=
XM_006710513.1:c.3312C=	XP_006710576.1:p.Ala1104=
XM_011541128.1:c.3339C=	XP_011539430.1:p.Ala1113=
XM_011541129.1:c.3147C=	XP_011539431.1:p.Ala1049=
XM_017000844.1:c.3509C=	XP_016856333.1:p.Pro1170=
XM_017000845.1:c.3506C=	XP_016856334.1:p.Pro1169=
XM_017000846.1:c.3482C=	XP_016856335.1:p.Pro1161=
XM_017000847.1:c.3479C=	XP_016856336.1:p.Pro1160=
XM_017000848.1:c.3407C=	XP_016856337.1:p.Pro1136=
XM_017000849.1:c.3392C=	XP_016856338.1:p.Pro1131=
XM_017000850.1:c.3317C=	XP_016856339.1:p.Pro1106=
NM_022089.4:c.3524C= MANE Select	NP_071372.1:p.Pro1175=
NM_001141973.3:c.3509C=	NP_001135445.1:p.Pro1170=
NM_001141974.3:c.3222C=	NP_001135446.1:p.Ala1074=