Canonical Allele Identifier: CA1156050563

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986913G= , CM000663.2:g.16986913G=	GRCh38
NC_000001.10:g.17313408G= , CM000663.1:g.17313408G=	GRCh37
NC_000001.9:g.17185995G=	NCBI36
NG_009054.1:g.30016C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3127C= MANE Select	ENSP00000327214.8:p.Pro1043=
ENST00000326735.12:c.3127C=	ENSP00000327214.8:p.Pro1043=
ENST00000341676.9:c.2995C=	ENSP00000341115.5:p.Pro999=
ENST00000452699.5:c.3112C=	ENSP00000413307.1:p.Pro1038=
ENST00000466561.1:n.1001C=
ENST00000502418.1:c.715C=	ENSP00000423065.1:p.Pro239=
NM_001141973.2:c.3112C=	NP_001135445.1:p.Pro1038=
NM_001141974.2:c.2995C=	NP_001135446.1:p.Pro999=
NM_022089.3:c.3127C=	NP_071372.1:p.Pro1043=
XM_005245809.1:c.3127C=	XP_005245866.1:p.Pro1043=
XM_005245810.1:c.3124C=	XP_005245867.1:p.Pro1042=
XM_005245811.1:c.3112C=	XP_005245868.1:p.Pro1038=
XM_005245812.1:c.3100C=	XP_005245869.1:p.Pro1034=
XM_005245813.1:c.3067C=	XP_005245870.1:p.Pro1023=
XM_005245815.1:c.3010C=	XP_005245872.1:p.Pro1004=
XM_006710512.1:c.3109C=	XP_006710575.1:p.Pro1037=
XM_006710513.1:c.3085C=	XP_006710576.1:p.Pro1029=
XM_011541128.1:c.3112C=	XP_011539430.1:p.Pro1038=
XM_011541129.1:c.2920C=	XP_011539431.1:p.Pro974=
XM_017000844.1:c.3112C=	XP_016856333.1:p.Pro1038=
XM_017000845.1:c.3109C=	XP_016856334.1:p.Pro1037=
XM_017000846.1:c.3085C=	XP_016856335.1:p.Pro1029=
XM_017000847.1:c.3082C=	XP_016856336.1:p.Pro1028=
XM_017000848.1:c.3010C=	XP_016856337.1:p.Pro1004=
XM_017000849.1:c.2995C=	XP_016856338.1:p.Pro999=
XM_017000850.1:c.2920C=	XP_016856339.1:p.Pro974=
NM_022089.4:c.3127C= MANE Select	NP_071372.1:p.Pro1043=
NM_001141973.3:c.3112C=	NP_001135445.1:p.Pro1038=
NM_001141974.3:c.2995C=	NP_001135446.1:p.Pro999=