Canonical Allele Identifier: CA1143780832

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986825C= , CM000663.2:g.16986825C=	GRCh38
NC_000001.10:g.17313320C= , CM000663.1:g.17313320C=	GRCh37
NC_000001.9:g.17185907C=	NCBI36
NG_009054.1:g.30104G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3215G= MANE Select	ENSP00000327214.8:p.Arg1072=
ENST00000326735.12:c.3215G=	ENSP00000327214.8:p.Arg1072=
ENST00000341676.9:c.3083G=	ENSP00000341115.5:p.Arg1028=
ENST00000452699.5:c.3200G=	ENSP00000413307.1:p.Arg1067=
ENST00000466561.1:n.1089G=
ENST00000502418.1:c.803G=	ENSP00000423065.1:p.Arg268=
NM_001141973.2:c.3200G=	NP_001135445.1:p.Arg1067=
NM_001141974.2:c.3083G=	NP_001135446.1:p.Arg1028=
NM_022089.3:c.3215G=	NP_071372.1:p.Arg1072=
XM_005245809.1:c.3215G=	XP_005245866.1:p.Arg1072=
XM_005245810.1:c.3212G=	XP_005245867.1:p.Arg1071=
XM_005245811.1:c.3200G=	XP_005245868.1:p.Arg1067=
XM_005245812.1:c.3188G=	XP_005245869.1:p.Arg1063=
XM_005245813.1:c.3155G=	XP_005245870.1:p.Arg1052=
XM_005245815.1:c.3098G=	XP_005245872.1:p.Arg1033=
XM_006710512.1:c.3197G=	XP_006710575.1:p.Arg1066=
XM_006710513.1:c.3173G=	XP_006710576.1:p.Arg1058=
XM_011541128.1:c.3200G=	XP_011539430.1:p.Arg1067=
XM_011541129.1:c.3008G=	XP_011539431.1:p.Arg1003=
XM_017000844.1:c.3200G=	XP_016856333.1:p.Arg1067=
XM_017000845.1:c.3197G=	XP_016856334.1:p.Arg1066=
XM_017000846.1:c.3173G=	XP_016856335.1:p.Arg1058=
XM_017000847.1:c.3170G=	XP_016856336.1:p.Arg1057=
XM_017000848.1:c.3098G=	XP_016856337.1:p.Arg1033=
XM_017000849.1:c.3083G=	XP_016856338.1:p.Arg1028=
XM_017000850.1:c.3008G=	XP_016856339.1:p.Arg1003=
NM_022089.4:c.3215G= MANE Select	NP_071372.1:p.Arg1072=
NM_001141973.3:c.3200G=	NP_001135445.1:p.Arg1067=
NM_001141974.3:c.3083G=	NP_001135446.1:p.Arg1028=