Canonical Allele Identifier: CA1156049502

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986305C= , CM000663.2:g.16986305C=	GRCh38
NC_000001.10:g.17312800C= , CM000663.1:g.17312800C=	GRCh37
NC_000001.9:g.17185387C=	NCBI36
NG_009054.1:g.30624G=
NG_029688.1:g.282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3459G= MANE Select	ENSP00000327214.8:p.Arg1153=
ENST00000326735.12:c.3459G=	ENSP00000327214.8:p.Arg1153=
ENST00000341676.9:c.3157G=	ENSP00000341115.5:p.Gly1053=
ENST00000452699.5:c.3444G=	ENSP00000413307.1:p.Arg1148=
ENST00000466561.1:n.1505G=
ENST00000502418.1:c.877G=	ENSP00000423065.1:p.Gly293=
NM_001141973.2:c.3444G=	NP_001135445.1:p.Arg1148=
NM_001141974.2:c.3157G=	NP_001135446.1:p.Gly1053=
NM_022089.3:c.3459G=	NP_071372.1:p.Arg1153=
XM_005245809.1:c.3289G=	XP_005245866.1:p.Gly1097=
XM_005245810.1:c.3286G=	XP_005245867.1:p.Gly1096=
XM_005245811.1:c.3274G=	XP_005245868.1:p.Gly1092=
XM_005245812.1:c.3262G=	XP_005245869.1:p.Gly1088=
XM_005245813.1:c.3229G=	XP_005245870.1:p.Gly1077=
XM_005245815.1:c.3172G=	XP_005245872.1:p.Gly1058=
XM_006710512.1:c.3271G=	XP_006710575.1:p.Gly1091=
XM_006710513.1:c.3247G=	XP_006710576.1:p.Gly1083=
XM_011541128.1:c.3274G=	XP_011539430.1:p.Gly1092=
XM_011541129.1:c.3082G=	XP_011539431.1:p.Gly1028=
XM_017000844.1:c.3444G=	XP_016856333.1:p.Arg1148=
XM_017000845.1:c.3441G=	XP_016856334.1:p.Arg1147=
XM_017000846.1:c.3417G=	XP_016856335.1:p.Arg1139=
XM_017000847.1:c.3414G=	XP_016856336.1:p.Arg1138=
XM_017000848.1:c.3342G=	XP_016856337.1:p.Arg1114=
XM_017000849.1:c.3327G=	XP_016856338.1:p.Arg1109=
XM_017000850.1:c.3252G=	XP_016856339.1:p.Arg1084=
NM_022089.4:c.3459G= MANE Select	NP_071372.1:p.Arg1153=
NM_001141973.3:c.3444G=	NP_001135445.1:p.Arg1148=
NM_001141974.3:c.3157G=	NP_001135446.1:p.Gly1053=