Canonical Allele Identifier: CA338233023
Gene: ATP13A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986561G>A , CM000663.2:g.16986561G>A GRCh38
NC_000001.10:g.17313056G>A , CM000663.1:g.17313056G>A GRCh37
NC_000001.9:g.17185643G>A NCBI36
NG_009054.1:g.30368C>T
NG_029688.1:g.26C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.3307C>T MANE Select ENSP00000327214.8:p.Gln1103Ter
ENST00000326735.12:c.3307C>T ENSP00000327214.8:p.Gln1103Ter
ENST00000341676.9:c.3104-203C>T ENSP00000341115.5:n.3104-203C>T
ENST00000452699.5:c.3292C>T ENSP00000413307.1:p.Gln1098Ter
ENST00000466561.1:n.1353C>T
ENST00000502418.1:c.824-203C>T ENSP00000423065.1:n.824-203C>T
NM_001141973.2:c.3292C>T NP_001135445.1:p.Gln1098Ter
NM_001141974.2:c.3104-203C>T NP_001135446.1:n.3104-203C>T
NM_022089.3:c.3307C>T NP_071372.1:p.Gln1103Ter
XM_005245809.1:c.3236-203C>T XP_005245866.1:n.3236-203C>T
XM_005245810.1:c.3233-203C>T XP_005245867.1:n.3233-203C>T
XM_005245811.1:c.3221-203C>T XP_005245868.1:n.3221-203C>T
XM_005245812.1:c.3209-203C>T XP_005245869.1:n.3209-203C>T
XM_005245813.1:c.3176-203C>T XP_005245870.1:n.3176-203C>T
XM_005245815.1:c.3119-203C>T XP_005245872.1:n.3119-203C>T
XM_006710512.1:c.3218-203C>T XP_006710575.1:n.3218-203C>T
XM_006710513.1:c.3194-203C>T XP_006710576.1:n.3194-203C>T
XM_011541128.1:c.3221-203C>T XP_011539430.1:n.3221-203C>T
XM_011541129.1:c.3029-203C>T XP_011539431.1:n.3029-203C>T
XM_017000844.1:c.3292C>T XP_016856333.1:p.Gln1098Ter
XM_017000845.1:c.3289C>T XP_016856334.1:p.Gln1097Ter
XM_017000846.1:c.3265C>T XP_016856335.1:p.Gln1089Ter
XM_017000847.1:c.3262C>T XP_016856336.1:p.Gln1088Ter
XM_017000848.1:c.3190C>T XP_016856337.1:p.Gln1064Ter
XM_017000849.1:c.3175C>T XP_016856338.1:p.Gln1059Ter
XM_017000850.1:c.3100C>T XP_016856339.1:p.Gln1034Ter
NM_022089.4:c.3307C>T MANE Select NP_071372.1:p.Gln1103Ter
NM_001141973.3:c.3292C>T NP_001135445.1:p.Gln1098Ter
NM_001141974.3:c.3104-203C>T NP_001135446.1:n.3104-203C>T