Canonical Allele Identifier: CA1141581613
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986833C= , CM000663.2:g.16986833C= GRCh38
NC_000001.10:g.17313328C= , CM000663.1:g.17313328C= GRCh37
NC_000001.9:g.17185915C= NCBI36
NG_009054.1:g.30096G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.3207G= MANE Select ENSP00000327214.8:p.Ala1069=
ENST00000326735.12:c.3207G= ENSP00000327214.8:p.Ala1069=
ENST00000341676.9:c.3075G= ENSP00000341115.5:p.Ala1025=
ENST00000452699.5:c.3192G= ENSP00000413307.1:p.Ala1064=
ENST00000466561.1:n.1081G=
ENST00000502418.1:c.795G= ENSP00000423065.1:p.Ala265=
NM_001141973.2:c.3192G= NP_001135445.1:p.Ala1064=
NM_001141974.2:c.3075G= NP_001135446.1:p.Ala1025=
NM_022089.3:c.3207G= NP_071372.1:p.Ala1069=
XM_005245809.1:c.3207G= XP_005245866.1:p.Ala1069=
XM_005245810.1:c.3204G= XP_005245867.1:p.Ala1068=
XM_005245811.1:c.3192G= XP_005245868.1:p.Ala1064=
XM_005245812.1:c.3180G= XP_005245869.1:p.Ala1060=
XM_005245813.1:c.3147G= XP_005245870.1:p.Ala1049=
XM_005245815.1:c.3090G= XP_005245872.1:p.Ala1030=
XM_006710512.1:c.3189G= XP_006710575.1:p.Ala1063=
XM_006710513.1:c.3165G= XP_006710576.1:p.Ala1055=
XM_011541128.1:c.3192G= XP_011539430.1:p.Ala1064=
XM_011541129.1:c.3000G= XP_011539431.1:p.Ala1000=
XM_017000844.1:c.3192G= XP_016856333.1:p.Ala1064=
XM_017000845.1:c.3189G= XP_016856334.1:p.Ala1063=
XM_017000846.1:c.3165G= XP_016856335.1:p.Ala1055=
XM_017000847.1:c.3162G= XP_016856336.1:p.Ala1054=
XM_017000848.1:c.3090G= XP_016856337.1:p.Ala1030=
XM_017000849.1:c.3075G= XP_016856338.1:p.Ala1025=
XM_017000850.1:c.3000G= XP_016856339.1:p.Ala1000=
NM_022089.4:c.3207G= MANE Select NP_071372.1:p.Ala1069=
NM_001141973.3:c.3192G= NP_001135445.1:p.Ala1064=
NM_001141974.3:c.3075G= NP_001135446.1:p.Ala1025=