Canonical Allele Identifier: CA1156021108
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16989760T= , CM000663.2:g.16989760T= GRCh38
NC_000001.10:g.17316255T= , CM000663.1:g.17316255T= GRCh37
NC_000001.9:g.17188842T= NCBI36
NG_009054.1:g.27169A=

Transcript Alleles

HGVS Amino-acid change
ENST00000326735.13:c.2540A= MANE Select ENSP00000327214.8:p.Gln847=
ENST00000326735.12:c.2540A= ENSP00000327214.8:p.Gln847=
ENST00000341676.9:c.2408A= ENSP00000341115.5:p.Gln803=
ENST00000452699.5:c.2525A= ENSP00000413307.1:p.Gln842=
ENST00000466561.1:n.414A=
ENST00000502418.1:c.128A= ENSP00000423065.1:p.Gln43=
NM_001141973.2:c.2525A= NP_001135445.1:p.Gln842=
NM_001141974.2:c.2408A= NP_001135446.1:p.Gln803=
NM_022089.3:c.2540A= NP_071372.1:p.Gln847=
XM_005245809.1:c.2540A= XP_005245866.1:p.Gln847=
XM_005245810.1:c.2537A= XP_005245867.1:p.Gln846=
XM_005245811.1:c.2525A= XP_005245868.1:p.Gln842=
XM_005245812.1:c.2513A= XP_005245869.1:p.Gln838=
XM_005245813.1:c.2480A= XP_005245870.1:p.Gln827=
XM_005245815.1:c.2423A= XP_005245872.1:p.Gln808=
XM_006710512.1:c.2522A= XP_006710575.1:p.Gln841=
XM_006710513.1:c.2498A= XP_006710576.1:p.Gln833=
XM_011541128.1:c.2525A= XP_011539430.1:p.Gln842=
XM_011541129.1:c.2333A= XP_011539431.1:p.Gln778=
XM_017000844.1:c.2525A= XP_016856333.1:p.Gln842=
XM_017000845.1:c.2522A= XP_016856334.1:p.Gln841=
XM_017000846.1:c.2498A= XP_016856335.1:p.Gln833=
XM_017000847.1:c.2495A= XP_016856336.1:p.Gln832=
XM_017000848.1:c.2423A= XP_016856337.1:p.Gln808=
XM_017000849.1:c.2408A= XP_016856338.1:p.Gln803=
XM_017000850.1:c.2333A= XP_016856339.1:p.Gln778=
NM_022089.4:c.2540A= MANE Select NP_071372.1:p.Gln847=
NM_001141973.3:c.2525A= NP_001135445.1:p.Gln842=
NM_001141974.3:c.2408A= NP_001135446.1:p.Gln803=