Canonical Allele Identifier: CA1156049967
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986609G= , CM000663.2:g.16986609G= GRCh38
NC_000001.10:g.17313104G= , CM000663.1:g.17313104G= GRCh37
NC_000001.9:g.17185691G= NCBI36
NG_009054.1:g.30320C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.3259C= MANE Select ENSP00000327214.8:p.Leu1087=
ENST00000326735.12:c.3259C= ENSP00000327214.8:p.Leu1087=
ENST00000341676.9:c.3103+196C= ENSP00000341115.5:n.3103+196C=
ENST00000452699.5:c.3244C= ENSP00000413307.1:p.Leu1082=
ENST00000466561.1:n.1305C=
ENST00000502418.1:c.823+196C= ENSP00000423065.1:n.823+196C=
NM_001141973.2:c.3244C= NP_001135445.1:p.Leu1082=
NM_001141974.2:c.3103+196C= NP_001135446.1:n.3103+196C=
NM_022089.3:c.3259C= NP_071372.1:p.Leu1087=
XM_005245809.1:c.3235+196C= XP_005245866.1:n.3235+196C=
XM_005245810.1:c.3232+196C= XP_005245867.1:n.3232+196C=
XM_005245811.1:c.3220+196C= XP_005245868.1:n.3220+196C=
XM_005245812.1:c.3208+196C= XP_005245869.1:n.3208+196C=
XM_005245813.1:c.3175+196C= XP_005245870.1:n.3175+196C=
XM_005245815.1:c.3118+196C= XP_005245872.1:n.3118+196C=
XM_006710512.1:c.3217+196C= XP_006710575.1:n.3217+196C=
XM_006710513.1:c.3193+196C= XP_006710576.1:n.3193+196C=
XM_011541128.1:c.3220+196C= XP_011539430.1:n.3220+196C=
XM_011541129.1:c.3028+196C= XP_011539431.1:n.3028+196C=
XM_017000844.1:c.3244C= XP_016856333.1:p.Leu1082=
XM_017000845.1:c.3241C= XP_016856334.1:p.Leu1081=
XM_017000846.1:c.3217C= XP_016856335.1:p.Leu1073=
XM_017000847.1:c.3214C= XP_016856336.1:p.Leu1072=
XM_017000848.1:c.3142C= XP_016856337.1:p.Leu1048=
XM_017000849.1:c.3127C= XP_016856338.1:p.Leu1043=
XM_017000850.1:c.3052C= XP_016856339.1:p.Leu1018=
NM_022089.4:c.3259C= MANE Select NP_071372.1:p.Leu1087=
NM_001141973.3:c.3244C= NP_001135445.1:p.Leu1082=
NM_001141974.3:c.3103+196C= NP_001135446.1:n.3103+196C=