Canonical Allele Identifier: CA338253136
Gene: ATP13A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16996264T>A , CM000663.2:g.16996264T>A GRCh38
NC_000001.10:g.17322759T>A , CM000663.1:g.17322759T>A GRCh37
NC_000001.9:g.17195346T>A NCBI36
NG_009054.1:g.20665A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.1343A>T MANE Select ENSP00000327214.8:p.Tyr448Phe
ENST00000326735.12:c.1343A>T ENSP00000327214.8:p.Tyr448Phe
ENST00000341676.9:c.1328A>T ENSP00000341115.5:p.Tyr443Phe
ENST00000452699.5:c.1328A>T ENSP00000413307.1:p.Tyr443Phe
ENST00000463860.5:n.951A>T
ENST00000502860.1:n.371A>T
ENST00000503552.1:c.20A>T ENSP00000421126.1:p.Tyr7Phe
ENST00000506174.5:c.485A>T ENSP00000424393.1:p.Tyr162Phe
ENST00000509392.1:n.431A>T
ENST00000617114.4:c.371A>T ENSP00000478781.1:p.Tyr124Phe
NM_001141973.2:c.1328A>T NP_001135445.1:p.Tyr443Phe
NM_001141974.2:c.1328A>T NP_001135446.1:p.Tyr443Phe
NM_022089.3:c.1343A>T NP_071372.1:p.Tyr448Phe
XM_005245809.1:c.1343A>T XP_005245866.1:p.Tyr448Phe
XM_005245810.1:c.1340A>T XP_005245867.1:p.Tyr447Phe
XM_005245811.1:c.1328A>T XP_005245868.1:p.Tyr443Phe
XM_005245812.1:c.1316A>T XP_005245869.1:p.Tyr439Phe
XM_005245813.1:c.1343A>T XP_005245870.1:p.Tyr448Phe
XM_005245815.1:c.1343A>T XP_005245872.1:p.Tyr448Phe
XM_006710512.1:c.1325A>T XP_006710575.1:p.Tyr442Phe
XM_006710513.1:c.1301A>T XP_006710576.1:p.Tyr434Phe
XM_011541128.1:c.1343A>T XP_011539430.1:p.Tyr448Phe
XM_011541129.1:c.1343A>T XP_011539431.1:p.Tyr448Phe
XM_017000844.1:c.1343A>T XP_016856333.1:p.Tyr448Phe
XM_017000845.1:c.1325A>T XP_016856334.1:p.Tyr442Phe
XM_017000846.1:c.1301A>T XP_016856335.1:p.Tyr434Phe
XM_017000847.1:c.1313A>T XP_016856336.1:p.Tyr438Phe
XM_017000848.1:c.1343A>T XP_016856337.1:p.Tyr448Phe
XM_017000849.1:c.1328A>T XP_016856338.1:p.Tyr443Phe
XM_017000850.1:c.1343A>T XP_016856339.1:p.Tyr448Phe
NM_022089.4:c.1343A>T MANE Select NP_071372.1:p.Tyr448Phe
NM_001141973.3:c.1328A>T NP_001135445.1:p.Tyr443Phe
NM_001141974.3:c.1328A>T NP_001135446.1:p.Tyr443Phe