Canonical Allele Identifier: CA1156049819

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986477C= , CM000663.2:g.16986477C=	GRCh38
NC_000001.10:g.17312972C= , CM000663.1:g.17312972C=	GRCh37
NC_000001.9:g.17185559C=	NCBI36
NG_009054.1:g.30452G=
NG_029688.1:g.110G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3391G= MANE Select	ENSP00000327214.8:p.Ala1131=
ENST00000326735.12:c.3391G=	ENSP00000327214.8:p.Ala1131=
ENST00000341676.9:c.3104-119G=	ENSP00000341115.5:n.3104-119G=
ENST00000452699.5:c.3376G=	ENSP00000413307.1:p.Ala1126=
ENST00000466561.1:n.1437G=
ENST00000502418.1:c.824-119G=	ENSP00000423065.1:n.824-119G=
NM_001141973.2:c.3376G=	NP_001135445.1:p.Ala1126=
NM_001141974.2:c.3104-119G=	NP_001135446.1:n.3104-119G=
NM_022089.3:c.3391G=	NP_071372.1:p.Ala1131=
XM_005245809.1:c.3236-119G=	XP_005245866.1:n.3236-119G=
XM_005245810.1:c.3233-119G=	XP_005245867.1:n.3233-119G=
XM_005245811.1:c.3221-119G=	XP_005245868.1:n.3221-119G=
XM_005245812.1:c.3209-119G=	XP_005245869.1:n.3209-119G=
XM_005245813.1:c.3176-119G=	XP_005245870.1:n.3176-119G=
XM_005245815.1:c.3119-119G=	XP_005245872.1:n.3119-119G=
XM_006710512.1:c.3218-119G=	XP_006710575.1:n.3218-119G=
XM_006710513.1:c.3194-119G=	XP_006710576.1:n.3194-119G=
XM_011541128.1:c.3221-119G=	XP_011539430.1:n.3221-119G=
XM_011541129.1:c.3029-119G=	XP_011539431.1:n.3029-119G=
XM_017000844.1:c.3376G=	XP_016856333.1:p.Ala1126=
XM_017000845.1:c.3373G=	XP_016856334.1:p.Ala1125=
XM_017000846.1:c.3349G=	XP_016856335.1:p.Ala1117=
XM_017000847.1:c.3346G=	XP_016856336.1:p.Ala1116=
XM_017000848.1:c.3274G=	XP_016856337.1:p.Ala1092=
XM_017000849.1:c.3259G=	XP_016856338.1:p.Ala1087=
XM_017000850.1:c.3184G=	XP_016856339.1:p.Ala1062=
NM_022089.4:c.3391G= MANE Select	NP_071372.1:p.Ala1131=
NM_001141973.3:c.3376G=	NP_001135445.1:p.Ala1126=
NM_001141974.3:c.3104-119G=	NP_001135446.1:n.3104-119G=