Canonical Allele Identifier: CA890931515
Gene: ATP13A2 HGNC NCBI

Linked Data

dbSNP Id: rs1448639232

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16989658G>A , CM000663.2:g.16989658G>A GRCh38
NC_000001.10:g.17316153G>A , CM000663.1:g.17316153G>A GRCh37
NC_000001.9:g.17188740G>A NCBI36
NG_009054.1:g.27271C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000326735.13:c.2609+33C>T MANE Select ENSP00000327214.8:n.2609+33C>T
ENST00000326735.12:c.2609+33C>T ENSP00000327214.8:n.2609+33C>T
ENST00000341676.9:c.2477+33C>T ENSP00000341115.5:n.2477+33C>T
ENST00000452699.5:c.2594+33C>T ENSP00000413307.1:n.2594+33C>T
ENST00000466561.1:n.483+33C>T
ENST00000502418.1:c.197+33C>T ENSP00000423065.1:n.197+33C>T
NM_001141973.2:c.2594+33C>T NP_001135445.1:n.2594+33C>T
NM_001141974.2:c.2477+33C>T NP_001135446.1:n.2477+33C>T
NM_022089.3:c.2609+33C>T NP_071372.1:n.2609+33C>T
XM_005245809.1:c.2609+33C>T XP_005245866.1:n.2609+33C>T
XM_005245810.1:c.2606+33C>T XP_005245867.1:n.2606+33C>T
XM_005245811.1:c.2594+33C>T XP_005245868.1:n.2594+33C>T
XM_005245812.1:c.2582+33C>T XP_005245869.1:n.2582+33C>T
XM_005245813.1:c.2549+33C>T XP_005245870.1:n.2549+33C>T
XM_005245815.1:c.2492+33C>T XP_005245872.1:n.2492+33C>T
XM_006710512.1:c.2591+33C>T XP_006710575.1:n.2591+33C>T
XM_006710513.1:c.2567+33C>T XP_006710576.1:n.2567+33C>T
XM_011541128.1:c.2594+33C>T XP_011539430.1:n.2594+33C>T
XM_011541129.1:c.2402+33C>T XP_011539431.1:n.2402+33C>T
XM_017000844.1:c.2594+33C>T XP_016856333.1:n.2594+33C>T
XM_017000845.1:c.2591+33C>T XP_016856334.1:n.2591+33C>T
XM_017000846.1:c.2567+33C>T XP_016856335.1:n.2567+33C>T
XM_017000847.1:c.2564+33C>T XP_016856336.1:n.2564+33C>T
XM_017000848.1:c.2492+33C>T XP_016856337.1:n.2492+33C>T
XM_017000849.1:c.2477+33C>T XP_016856338.1:n.2477+33C>T
XM_017000850.1:c.2402+33C>T XP_016856339.1:n.2402+33C>T
NM_022089.4:c.2609+33C>T MANE Select NP_071372.1:n.2609+33C>T
NM_001141973.3:c.2594+33C>T NP_001135445.1:n.2594+33C>T
NM_001141974.3:c.2477+33C>T NP_001135446.1:n.2477+33C>T