Canonical Allele Identifier: CA338231420
Gene: ATP13A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986158A>G , CM000663.2:g.16986158A>G GRCh38
NC_000001.10:g.17312653A>G , CM000663.1:g.17312653A>G GRCh37
NC_000001.9:g.17185240A>G NCBI36
NG_009054.1:g.30771T>C
NG_029688.1:g.429T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.*63T>C MANE Select ENSP00000327214.8:n.*63T>C
ENST00000326735.12:c.*63T>C ENSP00000327214.8:n.*63T>C
ENST00000341676.9:c.3304T>C ENSP00000341115.5:p.Ser1102Pro
ENST00000452699.5:c.*63T>C ENSP00000413307.1:n.*63T>C
ENST00000466561.1:n.1652T>C
ENST00000502418.1:c.1024T>C ENSP00000423065.1:p.Ser342Pro
NM_001141973.2:c.*63T>C NP_001135445.1:n.*63T>C
NM_001141974.2:c.3304T>C NP_001135446.1:p.Ser1102Pro
NM_022089.3:c.*63T>C NP_071372.1:n.*63T>C
XM_005245809.1:c.3436T>C XP_005245866.1:p.Ser1146Pro
XM_005245810.1:c.3433T>C XP_005245867.1:p.Ser1145Pro
XM_005245811.1:c.3421T>C XP_005245868.1:p.Ser1141Pro
XM_005245812.1:c.3409T>C XP_005245869.1:p.Ser1137Pro
XM_005245813.1:c.3376T>C XP_005245870.1:p.Ser1126Pro
XM_005245815.1:c.3319T>C XP_005245872.1:p.Ser1107Pro
XM_006710512.1:c.3418T>C XP_006710575.1:p.Ser1140Pro
XM_006710513.1:c.3394T>C XP_006710576.1:p.Ser1132Pro
XM_011541128.1:c.3421T>C XP_011539430.1:p.Ser1141Pro
XM_011541129.1:c.3229T>C XP_011539431.1:p.Ser1077Pro
XM_017000844.1:c.*63T>C XP_016856333.1:n.*63T>C
XM_017000845.1:c.*63T>C XP_016856334.1:n.*63T>C
XM_017000846.1:c.*63T>C XP_016856335.1:n.*63T>C
XM_017000847.1:c.*63T>C XP_016856336.1:n.*63T>C
XM_017000848.1:c.*63T>C XP_016856337.1:n.*63T>C
XM_017000849.1:c.*63T>C XP_016856338.1:n.*63T>C
XM_017000850.1:c.*63T>C XP_016856339.1:n.*63T>C
NM_022089.4:c.*63T>C MANE Select NP_071372.1:n.*63T>C
NM_001141973.3:c.*63T>C NP_001135445.1:n.*63T>C
NM_001141974.3:c.3304T>C NP_001135446.1:p.Ser1102Pro