Canonical Allele Identifier: CA1156048726

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986052G= , CM000663.2:g.16986052G=	GRCh38
NC_000001.10:g.17312547G= , CM000663.1:g.17312547G=	GRCh37
NC_000001.9:g.17185134G=	NCBI36
NG_009054.1:g.30877C=
NG_029688.1:g.535C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.*169C= MANE Select	ENSP00000327214.8:n.*169C=
ENST00000326735.12:c.*169C=	ENSP00000327214.8:n.*169C=
ENST00000341676.9:c.3410C=	ENSP00000341115.5:p.Pro1137=
ENST00000452699.5:c.*169C=	ENSP00000413307.1:n.*169C=
ENST00000466561.1:n.1758C=
ENST00000502418.1:c.1130C=	ENSP00000423065.1:p.Pro377=
NM_001141973.2:c.*169C=	NP_001135445.1:n.*169C=
NM_001141974.2:c.3410C=	NP_001135446.1:p.Pro1137=
NM_022089.3:c.*169C=	NP_071372.1:n.*169C=
XM_005245809.1:c.3542C=	XP_005245866.1:p.Pro1181=
XM_005245810.1:c.3539C=	XP_005245867.1:p.Pro1180=
XM_005245811.1:c.3527C=	XP_005245868.1:p.Pro1176=
XM_005245812.1:c.3515C=	XP_005245869.1:p.Pro1172=
XM_005245813.1:c.3482C=	XP_005245870.1:p.Pro1161=
XM_005245815.1:c.3425C=	XP_005245872.1:p.Pro1142=
XM_006710512.1:c.3524C=	XP_006710575.1:p.Pro1175=
XM_006710513.1:c.3500C=	XP_006710576.1:p.Pro1167=
XM_011541128.1:c.3527C=	XP_011539430.1:p.Pro1176=
XM_011541129.1:c.3335C=	XP_011539431.1:p.Pro1112=
XM_017000844.1:c.*169C=	XP_016856333.1:n.*169C=
XM_017000845.1:c.*169C=	XP_016856334.1:n.*169C=
XM_017000846.1:c.*169C=	XP_016856335.1:n.*169C=
XM_017000847.1:c.*169C=	XP_016856336.1:n.*169C=
XM_017000848.1:c.*169C=	XP_016856337.1:n.*169C=
XM_017000849.1:c.*169C=	XP_016856338.1:n.*169C=
XM_017000850.1:c.*169C=	XP_016856339.1:n.*169C=
NM_022089.4:c.*169C= MANE Select	NP_071372.1:n.*169C=
NM_001141973.3:c.*169C=	NP_001135445.1:n.*169C=
NM_001141974.3:c.3410C=	NP_001135446.1:p.Pro1137=