Canonical Allele Identifier: CA1156050089
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986696G= , CM000663.2:g.16986696G= GRCh38
NC_000001.10:g.17313191G= , CM000663.1:g.17313191G= GRCh37
NC_000001.9:g.17185778G= NCBI36
NG_009054.1:g.30233C=

Transcript Alleles

HGVS Amino-acid change
ENST00000326735.13:c.3236-64C= MANE Select ENSP00000327214.8:n.3236-64C=
ENST00000326735.12:c.3236-64C= ENSP00000327214.8:n.3236-64C=
ENST00000341676.9:c.3103+109C= ENSP00000341115.5:n.3103+109C=
ENST00000452699.5:c.3221-64C= ENSP00000413307.1:n.3221-64C=
ENST00000466561.1:n.1218C=
ENST00000502418.1:c.823+109C= ENSP00000423065.1:n.823+109C=
NM_001141973.2:c.3221-64C= NP_001135445.1:n.3221-64C=
NM_001141974.2:c.3103+109C= NP_001135446.1:n.3103+109C=
NM_022089.3:c.3236-64C= NP_071372.1:n.3236-64C=
XM_005245809.1:c.3235+109C= XP_005245866.1:n.3235+109C=
XM_005245810.1:c.3232+109C= XP_005245867.1:n.3232+109C=
XM_005245811.1:c.3220+109C= XP_005245868.1:n.3220+109C=
XM_005245812.1:c.3208+109C= XP_005245869.1:n.3208+109C=
XM_005245813.1:c.3175+109C= XP_005245870.1:n.3175+109C=
XM_005245815.1:c.3118+109C= XP_005245872.1:n.3118+109C=
XM_006710512.1:c.3217+109C= XP_006710575.1:n.3217+109C=
XM_006710513.1:c.3193+109C= XP_006710576.1:n.3193+109C=
XM_011541128.1:c.3220+109C= XP_011539430.1:n.3220+109C=
XM_011541129.1:c.3028+109C= XP_011539431.1:n.3028+109C=
XM_017000844.1:c.3221-64C= XP_016856333.1:n.3221-64C=
XM_017000845.1:c.3218-64C= XP_016856334.1:n.3218-64C=
XM_017000846.1:c.3194-64C= XP_016856335.1:n.3194-64C=
XM_017000847.1:c.3191-64C= XP_016856336.1:n.3191-64C=
XM_017000848.1:c.3119-64C= XP_016856337.1:n.3119-64C=
XM_017000849.1:c.3104-64C= XP_016856338.1:n.3104-64C=
XM_017000850.1:c.3029-64C= XP_016856339.1:n.3029-64C=
NM_022089.4:c.3236-64C= MANE Select NP_071372.1:n.3236-64C=
NM_001141973.3:c.3221-64C= NP_001135445.1:n.3221-64C=
NM_001141974.3:c.3103+109C= NP_001135446.1:n.3103+109C=