Canonical Allele Identifier: CA1156021014

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989709C= , CM000663.2:g.16989709C=	GRCh38
NC_000001.10:g.17316204C= , CM000663.1:g.17316204C=	GRCh37
NC_000001.9:g.17188791C=	NCBI36
NG_009054.1:g.27220G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.2591G= MANE Select	ENSP00000327214.8:p.Cys864=
ENST00000326735.12:c.2591G=	ENSP00000327214.8:p.Cys864=
ENST00000341676.9:c.2459G=	ENSP00000341115.5:p.Cys820=
ENST00000452699.5:c.2576G=	ENSP00000413307.1:p.Cys859=
ENST00000466561.1:n.465G=
ENST00000502418.1:c.179G=	ENSP00000423065.1:p.Cys60=
NM_001141973.2:c.2576G=	NP_001135445.1:p.Cys859=
NM_001141974.2:c.2459G=	NP_001135446.1:p.Cys820=
NM_022089.3:c.2591G=	NP_071372.1:p.Cys864=
XM_005245809.1:c.2591G=	XP_005245866.1:p.Cys864=
XM_005245810.1:c.2588G=	XP_005245867.1:p.Cys863=
XM_005245811.1:c.2576G=	XP_005245868.1:p.Cys859=
XM_005245812.1:c.2564G=	XP_005245869.1:p.Cys855=
XM_005245813.1:c.2531G=	XP_005245870.1:p.Cys844=
XM_005245815.1:c.2474G=	XP_005245872.1:p.Cys825=
XM_006710512.1:c.2573G=	XP_006710575.1:p.Cys858=
XM_006710513.1:c.2549G=	XP_006710576.1:p.Cys850=
XM_011541128.1:c.2576G=	XP_011539430.1:p.Cys859=
XM_011541129.1:c.2384G=	XP_011539431.1:p.Cys795=
XM_017000844.1:c.2576G=	XP_016856333.1:p.Cys859=
XM_017000845.1:c.2573G=	XP_016856334.1:p.Cys858=
XM_017000846.1:c.2549G=	XP_016856335.1:p.Cys850=
XM_017000847.1:c.2546G=	XP_016856336.1:p.Cys849=
XM_017000848.1:c.2474G=	XP_016856337.1:p.Cys825=
XM_017000849.1:c.2459G=	XP_016856338.1:p.Cys820=
XM_017000850.1:c.2384G=	XP_016856339.1:p.Cys795=
NM_022089.4:c.2591G= MANE Select	NP_071372.1:p.Cys864=
NM_001141973.3:c.2576G=	NP_001135445.1:p.Cys859=
NM_001141974.3:c.2459G=	NP_001135446.1:p.Cys820=