Canonical Allele Identifier: CA1142028250
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17004738T= , CM000663.2:g.17004738T= GRCh38
NC_000001.10:g.17331233T= , CM000663.1:g.17331233T= GRCh37
NC_000001.9:g.17203820T= NCBI36
NG_009054.1:g.12191A=

Transcript Alleles

HGVS Amino-acid change
ENST00000326735.13:c.431A= MANE Select ENSP00000327214.8:p.Asp144=
ENST00000326735.12:c.431A= ENSP00000327214.8:p.Asp144=
ENST00000341676.9:c.431A= ENSP00000341115.5:p.Asp144=
ENST00000452699.5:c.431A= ENSP00000413307.1:p.Asp144=
ENST00000508222.5:c.165A=
ENST00000509619.1:c.408A=
ENST00000510069.5:c.357A=
ENST00000511957.5:c.143A= ENSP00000427241.1:p.Asp48=
ENST00000617114.4:c.-416A= ENSP00000478781.1:n.-416A=
NM_001141973.2:c.431A= NP_001135445.1:p.Asp144=
NM_001141974.2:c.431A= NP_001135446.1:p.Asp144=
NM_022089.3:c.431A= NP_071372.1:p.Asp144=
XM_005245809.1:c.431A= XP_005245866.1:p.Asp144=
XM_005245810.1:c.431A= XP_005245867.1:p.Asp144=
XM_005245811.1:c.431A= XP_005245868.1:p.Asp144=
XM_005245812.1:c.431A= XP_005245869.1:p.Asp144=
XM_005245813.1:c.431A= XP_005245870.1:p.Asp144=
XM_005245815.1:c.431A= XP_005245872.1:p.Asp144=
XM_006710512.1:c.431A= XP_006710575.1:p.Asp144=
XM_006710513.1:c.431A= XP_006710576.1:p.Asp144=
XM_011541128.1:c.431A= XP_011539430.1:p.Asp144=
XM_011541129.1:c.431A= XP_011539431.1:p.Asp144=
XM_017000844.1:c.431A= XP_016856333.1:p.Asp144=
XM_017000845.1:c.431A= XP_016856334.1:p.Asp144=
XM_017000846.1:c.431A= XP_016856335.1:p.Asp144=
XM_017000847.1:c.431A= XP_016856336.1:p.Asp144=
XM_017000848.1:c.431A= XP_016856337.1:p.Asp144=
XM_017000849.1:c.431A= XP_016856338.1:p.Asp144=
XM_017000850.1:c.431A= XP_016856339.1:p.Asp144=
NM_022089.4:c.431A= MANE Select NP_071372.1:p.Asp144=
NM_001141973.3:c.431A= NP_001135445.1:p.Asp144=
NM_001141974.3:c.431A= NP_001135446.1:p.Asp144=