Canonical Allele Identifier: CA1156049263
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986234C= , CM000663.2:g.16986234C= GRCh38
NC_000001.10:g.17312729C= , CM000663.1:g.17312729C= GRCh37
NC_000001.9:g.17185316C= NCBI36
NG_009054.1:g.30695G=
NG_029688.1:g.353G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.3530G= MANE Select ENSP00000327214.8:p.Gly1177=
ENST00000326735.12:c.3530G= ENSP00000327214.8:p.Gly1177=
ENST00000341676.9:c.3228G= ENSP00000341115.5:p.Arg1076=
ENST00000452699.5:c.3515G= ENSP00000413307.1:p.Gly1172=
ENST00000466561.1:n.1576G=
ENST00000502418.1:c.948G= ENSP00000423065.1:p.Arg316=
NM_001141973.2:c.3515G= NP_001135445.1:p.Gly1172=
NM_001141974.2:c.3228G= NP_001135446.1:p.Arg1076=
NM_022089.3:c.3530G= NP_071372.1:p.Gly1177=
XM_005245809.1:c.3360G= XP_005245866.1:p.Arg1120=
XM_005245810.1:c.3357G= XP_005245867.1:p.Arg1119=
XM_005245811.1:c.3345G= XP_005245868.1:p.Arg1115=
XM_005245812.1:c.3333G= XP_005245869.1:p.Arg1111=
XM_005245813.1:c.3300G= XP_005245870.1:p.Arg1100=
XM_005245815.1:c.3243G= XP_005245872.1:p.Arg1081=
XM_006710512.1:c.3342G= XP_006710575.1:p.Arg1114=
XM_006710513.1:c.3318G= XP_006710576.1:p.Arg1106=
XM_011541128.1:c.3345G= XP_011539430.1:p.Arg1115=
XM_011541129.1:c.3153G= XP_011539431.1:p.Arg1051=
XM_017000844.1:c.3515G= XP_016856333.1:p.Gly1172=
XM_017000845.1:c.3512G= XP_016856334.1:p.Gly1171=
XM_017000846.1:c.3488G= XP_016856335.1:p.Gly1163=
XM_017000847.1:c.3485G= XP_016856336.1:p.Gly1162=
XM_017000848.1:c.3413G= XP_016856337.1:p.Gly1138=
XM_017000849.1:c.3398G= XP_016856338.1:p.Gly1133=
XM_017000850.1:c.3323G= XP_016856339.1:p.Gly1108=
NM_022089.4:c.3530G= MANE Select NP_071372.1:p.Gly1177=
NM_001141973.3:c.3515G= NP_001135445.1:p.Gly1172=
NM_001141974.3:c.3228G= NP_001135446.1:p.Arg1076=