Canonical Allele Identifier: CA1156049634
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986356G= , CM000663.2:g.16986356G= GRCh38
NC_000001.10:g.17312851G= , CM000663.1:g.17312851G= GRCh37
NC_000001.9:g.17185438G= NCBI36
NG_009054.1:g.30573C=
NG_029688.1:g.231C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.3408C= MANE Select ENSP00000327214.8:p.Ser1136=
ENST00000326735.12:c.3408C= ENSP00000327214.8:p.Ser1136=
ENST00000341676.9:c.3106C= ENSP00000341115.5:p.Arg1036=
ENST00000452699.5:c.3393C= ENSP00000413307.1:p.Ser1131=
ENST00000466561.1:n.1454C=
ENST00000502418.1:c.826C= ENSP00000423065.1:p.Arg276=
NM_001141973.2:c.3393C= NP_001135445.1:p.Ser1131=
NM_001141974.2:c.3106C= NP_001135446.1:p.Arg1036=
NM_022089.3:c.3408C= NP_071372.1:p.Ser1136=
XM_005245809.1:c.3238C= XP_005245866.1:p.Arg1080=
XM_005245810.1:c.3235C= XP_005245867.1:p.Arg1079=
XM_005245811.1:c.3223C= XP_005245868.1:p.Arg1075=
XM_005245812.1:c.3211C= XP_005245869.1:p.Arg1071=
XM_005245813.1:c.3178C= XP_005245870.1:p.Arg1060=
XM_005245815.1:c.3121C= XP_005245872.1:p.Arg1041=
XM_006710512.1:c.3220C= XP_006710575.1:p.Arg1074=
XM_006710513.1:c.3196C= XP_006710576.1:p.Arg1066=
XM_011541128.1:c.3223C= XP_011539430.1:p.Arg1075=
XM_011541129.1:c.3031C= XP_011539431.1:p.Arg1011=
XM_017000844.1:c.3393C= XP_016856333.1:p.Ser1131=
XM_017000845.1:c.3390C= XP_016856334.1:p.Ser1130=
XM_017000846.1:c.3366C= XP_016856335.1:p.Ser1122=
XM_017000847.1:c.3363C= XP_016856336.1:p.Ser1121=
XM_017000848.1:c.3291C= XP_016856337.1:p.Ser1097=
XM_017000849.1:c.3276C= XP_016856338.1:p.Ser1092=
XM_017000850.1:c.3201C= XP_016856339.1:p.Ser1067=
NM_022089.4:c.3408C= MANE Select NP_071372.1:p.Ser1136=
NM_001141973.3:c.3393C= NP_001135445.1:p.Ser1131=
NM_001141974.3:c.3106C= NP_001135446.1:p.Arg1036=