Canonical Allele Identifier: CA1156050546
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986906T= , CM000663.2:g.16986906T= GRCh38
NC_000001.10:g.17313401T= , CM000663.1:g.17313401T= GRCh37
NC_000001.9:g.17185988T= NCBI36
NG_009054.1:g.30023A=

Transcript Alleles

HGVS Amino-acid change
ENST00000326735.13:c.3134A= MANE Select ENSP00000327214.8:p.Tyr1045=
ENST00000326735.12:c.3134A= ENSP00000327214.8:p.Tyr1045=
ENST00000341676.9:c.3002A= ENSP00000341115.5:p.Tyr1001=
ENST00000452699.5:c.3119A= ENSP00000413307.1:p.Tyr1040=
ENST00000466561.1:n.1008A=
ENST00000502418.1:c.722A= ENSP00000423065.1:p.Tyr241=
NM_001141973.2:c.3119A= NP_001135445.1:p.Tyr1040=
NM_001141974.2:c.3002A= NP_001135446.1:p.Tyr1001=
NM_022089.3:c.3134A= NP_071372.1:p.Tyr1045=
XM_005245809.1:c.3134A= XP_005245866.1:p.Tyr1045=
XM_005245810.1:c.3131A= XP_005245867.1:p.Tyr1044=
XM_005245811.1:c.3119A= XP_005245868.1:p.Tyr1040=
XM_005245812.1:c.3107A= XP_005245869.1:p.Tyr1036=
XM_005245813.1:c.3074A= XP_005245870.1:p.Tyr1025=
XM_005245815.1:c.3017A= XP_005245872.1:p.Tyr1006=
XM_006710512.1:c.3116A= XP_006710575.1:p.Tyr1039=
XM_006710513.1:c.3092A= XP_006710576.1:p.Tyr1031=
XM_011541128.1:c.3119A= XP_011539430.1:p.Tyr1040=
XM_011541129.1:c.2927A= XP_011539431.1:p.Tyr976=
XM_017000844.1:c.3119A= XP_016856333.1:p.Tyr1040=
XM_017000845.1:c.3116A= XP_016856334.1:p.Tyr1039=
XM_017000846.1:c.3092A= XP_016856335.1:p.Tyr1031=
XM_017000847.1:c.3089A= XP_016856336.1:p.Tyr1030=
XM_017000848.1:c.3017A= XP_016856337.1:p.Tyr1006=
XM_017000849.1:c.3002A= XP_016856338.1:p.Tyr1001=
XM_017000850.1:c.2927A= XP_016856339.1:p.Tyr976=
NM_022089.4:c.3134A= MANE Select NP_071372.1:p.Tyr1045=
NM_001141973.3:c.3119A= NP_001135445.1:p.Tyr1040=
NM_001141974.3:c.3002A= NP_001135446.1:p.Tyr1001=