Canonical Allele Identifier: CA1141580610
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986615_16986617delinsGGG , CM000663.2:g.16986615_16986617delinsGGG GRCh38
NC_000001.10:g.17313110_17313112delinsGGG , CM000663.1:g.17313110_17313112delinsGGG GRCh37
NC_000001.9:g.17185697_17185699delinsGGG NCBI36
NG_009054.1:g.30312_30314delinsCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000326735.13:c.3251_3253delinsCCC MANE Select ENSP00000327214.8:p.Ala1084=
ENST00000326735.12:c.3251_3253delinsCCC ENSP00000327214.8:p.Ala1084=
ENST00000341676.9:c.3103+188_3103+190delinsCCC ENSP00000341115.5:n.3103+188_3103+190deli...
ENST00000452699.5:c.3236_3238delinsCCC ENSP00000413307.1:p.Ala1079=
ENST00000466561.1:n.1297_1299delinsCCC
ENST00000502418.1:c.823+188_823+190delinsCCC ENSP00000423065.1:n.823+188_823+190delins...
NM_001141973.2:c.3236_3238delinsCCC NP_001135445.1:p.Ala1079=
NM_001141974.2:c.3103+188_3103+190delinsCCC NP_001135446.1:n.3103+188_3103+190delinsC...
NM_022089.3:c.3251_3253delinsCCC NP_071372.1:p.Ala1084=
XM_005245809.1:c.3235+188_3235+190delinsCCC XP_005245866.1:n.3235+188_3235+190delinsC...
XM_005245810.1:c.3232+188_3232+190delinsCCC XP_005245867.1:n.3232+188_3232+190delinsC...
XM_005245811.1:c.3220+188_3220+190delinsCCC XP_005245868.1:n.3220+188_3220+190delinsC...
XM_005245812.1:c.3208+188_3208+190delinsCCC XP_005245869.1:n.3208+188_3208+190delinsC...
XM_005245813.1:c.3175+188_3175+190delinsCCC XP_005245870.1:n.3175+188_3175+190delinsC...
XM_005245815.1:c.3118+188_3118+190delinsCCC XP_005245872.1:n.3118+188_3118+190delinsC...
XM_006710512.1:c.3217+188_3217+190delinsCCC XP_006710575.1:n.3217+188_3217+190delinsC...
XM_006710513.1:c.3193+188_3193+190delinsCCC XP_006710576.1:n.3193+188_3193+190delinsC...
XM_011541128.1:c.3220+188_3220+190delinsCCC XP_011539430.1:n.3220+188_3220+190delinsC...
XM_011541129.1:c.3028+188_3028+190delinsCCC XP_011539431.1:n.3028+188_3028+190delinsC...
XM_017000844.1:c.3236_3238delinsCCC XP_016856333.1:p.Ala1079=
XM_017000845.1:c.3233_3235delinsCCC XP_016856334.1:p.Ala1078=
XM_017000846.1:c.3209_3211delinsCCC XP_016856335.1:p.Ala1070=
XM_017000847.1:c.3206_3208delinsCCC XP_016856336.1:p.Ala1069=
XM_017000848.1:c.3134_3136delinsCCC XP_016856337.1:p.Ala1045=
XM_017000849.1:c.3119_3121delinsCCC XP_016856338.1:p.Ala1040=
XM_017000850.1:c.3044_3046delinsCCC XP_016856339.1:p.Ala1015=
NM_022089.4:c.3251_3253delinsCCC MANE Select NP_071372.1:p.Ala1084=
NM_001141973.3:c.3236_3238delinsCCC NP_001135445.1:p.Ala1079=
NM_001141974.3:c.3103+188_3103+190delinsCCC NP_001135446.1:n.3103+188_3103+190delinsC...