Canonical Allele Identifier: CA1156021035

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989726C= , CM000663.2:g.16989726C=	GRCh38
NC_000001.10:g.17316221C= , CM000663.1:g.17316221C=	GRCh37
NC_000001.9:g.17188808C=	NCBI36
NG_009054.1:g.27203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.2574G= MANE Select	ENSP00000327214.8:p.Gln858=
ENST00000326735.12:c.2574G=	ENSP00000327214.8:p.Gln858=
ENST00000341676.9:c.2442G=	ENSP00000341115.5:p.Gln814=
ENST00000452699.5:c.2559G=	ENSP00000413307.1:p.Gln853=
ENST00000466561.1:n.448G=
ENST00000502418.1:c.162G=	ENSP00000423065.1:p.Gln54=
NM_001141973.2:c.2559G=	NP_001135445.1:p.Gln853=
NM_001141974.2:c.2442G=	NP_001135446.1:p.Gln814=
NM_022089.3:c.2574G=	NP_071372.1:p.Gln858=
XM_005245809.1:c.2574G=	XP_005245866.1:p.Gln858=
XM_005245810.1:c.2571G=	XP_005245867.1:p.Gln857=
XM_005245811.1:c.2559G=	XP_005245868.1:p.Gln853=
XM_005245812.1:c.2547G=	XP_005245869.1:p.Gln849=
XM_005245813.1:c.2514G=	XP_005245870.1:p.Gln838=
XM_005245815.1:c.2457G=	XP_005245872.1:p.Gln819=
XM_006710512.1:c.2556G=	XP_006710575.1:p.Gln852=
XM_006710513.1:c.2532G=	XP_006710576.1:p.Gln844=
XM_011541128.1:c.2559G=	XP_011539430.1:p.Gln853=
XM_011541129.1:c.2367G=	XP_011539431.1:p.Gln789=
XM_017000844.1:c.2559G=	XP_016856333.1:p.Gln853=
XM_017000845.1:c.2556G=	XP_016856334.1:p.Gln852=
XM_017000846.1:c.2532G=	XP_016856335.1:p.Gln844=
XM_017000847.1:c.2529G=	XP_016856336.1:p.Gln843=
XM_017000848.1:c.2457G=	XP_016856337.1:p.Gln819=
XM_017000849.1:c.2442G=	XP_016856338.1:p.Gln814=
XM_017000850.1:c.2367G=	XP_016856339.1:p.Gln789=
NM_022089.4:c.2574G= MANE Select	NP_071372.1:p.Gln858=
NM_001141973.3:c.2559G=	NP_001135445.1:p.Gln853=
NM_001141974.3:c.2442G=	NP_001135446.1:p.Gln814=