Canonical Allele Identifier: CA1156048792
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986077G= , CM000663.2:g.16986077G= GRCh38
NC_000001.10:g.17312572G= , CM000663.1:g.17312572G= GRCh37
NC_000001.9:g.17185159G= NCBI36
NG_009054.1:g.30852C=
NG_029688.1:g.510C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.*144C= MANE Select ENSP00000327214.8:n.*144C=
ENST00000326735.12:c.*144C= ENSP00000327214.8:n.*144C=
ENST00000341676.9:c.3385C= ENSP00000341115.5:p.Pro1129=
ENST00000452699.5:c.*144C= ENSP00000413307.1:n.*144C=
ENST00000466561.1:n.1733C=
ENST00000502418.1:c.1105C= ENSP00000423065.1:p.Pro369=
NM_001141973.2:c.*144C= NP_001135445.1:n.*144C=
NM_001141974.2:c.3385C= NP_001135446.1:p.Pro1129=
NM_022089.3:c.*144C= NP_071372.1:n.*144C=
XM_005245809.1:c.3517C= XP_005245866.1:p.Pro1173=
XM_005245810.1:c.3514C= XP_005245867.1:p.Pro1172=
XM_005245811.1:c.3502C= XP_005245868.1:p.Pro1168=
XM_005245812.1:c.3490C= XP_005245869.1:p.Pro1164=
XM_005245813.1:c.3457C= XP_005245870.1:p.Pro1153=
XM_005245815.1:c.3400C= XP_005245872.1:p.Pro1134=
XM_006710512.1:c.3499C= XP_006710575.1:p.Pro1167=
XM_006710513.1:c.3475C= XP_006710576.1:p.Pro1159=
XM_011541128.1:c.3502C= XP_011539430.1:p.Pro1168=
XM_011541129.1:c.3310C= XP_011539431.1:p.Pro1104=
XM_017000844.1:c.*144C= XP_016856333.1:n.*144C=
XM_017000845.1:c.*144C= XP_016856334.1:n.*144C=
XM_017000846.1:c.*144C= XP_016856335.1:n.*144C=
XM_017000847.1:c.*144C= XP_016856336.1:n.*144C=
XM_017000848.1:c.*144C= XP_016856337.1:n.*144C=
XM_017000849.1:c.*144C= XP_016856338.1:n.*144C=
XM_017000850.1:c.*144C= XP_016856339.1:n.*144C=
NM_022089.4:c.*144C= MANE Select NP_071372.1:n.*144C=
NM_001141973.3:c.*144C= NP_001135445.1:n.*144C=
NM_001141974.3:c.3385C= NP_001135446.1:p.Pro1129=