Canonical Allele Identifier: CA1156049979
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986615G= , CM000663.2:g.16986615G= GRCh38
NC_000001.10:g.17313110G= , CM000663.1:g.17313110G= GRCh37
NC_000001.9:g.17185697G= NCBI36
NG_009054.1:g.30314C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.3253C= MANE Select ENSP00000327214.8:p.Leu1085=
ENST00000326735.12:c.3253C= ENSP00000327214.8:p.Leu1085=
ENST00000341676.9:c.3103+190C= ENSP00000341115.5:n.3103+190C=
ENST00000452699.5:c.3238C= ENSP00000413307.1:p.Leu1080=
ENST00000466561.1:n.1299C=
ENST00000502418.1:c.823+190C= ENSP00000423065.1:n.823+190C=
NM_001141973.2:c.3238C= NP_001135445.1:p.Leu1080=
NM_001141974.2:c.3103+190C= NP_001135446.1:n.3103+190C=
NM_022089.3:c.3253C= NP_071372.1:p.Leu1085=
XM_005245809.1:c.3235+190C= XP_005245866.1:n.3235+190C=
XM_005245810.1:c.3232+190C= XP_005245867.1:n.3232+190C=
XM_005245811.1:c.3220+190C= XP_005245868.1:n.3220+190C=
XM_005245812.1:c.3208+190C= XP_005245869.1:n.3208+190C=
XM_005245813.1:c.3175+190C= XP_005245870.1:n.3175+190C=
XM_005245815.1:c.3118+190C= XP_005245872.1:n.3118+190C=
XM_006710512.1:c.3217+190C= XP_006710575.1:n.3217+190C=
XM_006710513.1:c.3193+190C= XP_006710576.1:n.3193+190C=
XM_011541128.1:c.3220+190C= XP_011539430.1:n.3220+190C=
XM_011541129.1:c.3028+190C= XP_011539431.1:n.3028+190C=
XM_017000844.1:c.3238C= XP_016856333.1:p.Leu1080=
XM_017000845.1:c.3235C= XP_016856334.1:p.Leu1079=
XM_017000846.1:c.3211C= XP_016856335.1:p.Leu1071=
XM_017000847.1:c.3208C= XP_016856336.1:p.Leu1070=
XM_017000848.1:c.3136C= XP_016856337.1:p.Leu1046=
XM_017000849.1:c.3121C= XP_016856338.1:p.Leu1041=
XM_017000850.1:c.3046C= XP_016856339.1:p.Leu1016=
NM_022089.4:c.3253C= MANE Select NP_071372.1:p.Leu1085=
NM_001141973.3:c.3238C= NP_001135445.1:p.Leu1080=
NM_001141974.3:c.3103+190C= NP_001135446.1:n.3103+190C=