Canonical Allele Identifier: CA1156050328

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986810G= , CM000663.2:g.16986810G=	GRCh38
NC_000001.10:g.17313305G= , CM000663.1:g.17313305G=	GRCh37
NC_000001.9:g.17185892G=	NCBI36
NG_009054.1:g.30119C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.3230C= MANE Select	ENSP00000327214.8:p.Thr1077=
ENST00000326735.12:c.3230C=	ENSP00000327214.8:p.Thr1077=
ENST00000341676.9:c.3098C=	ENSP00000341115.5:p.Thr1033=
ENST00000452699.5:c.3215C=	ENSP00000413307.1:p.Thr1072=
ENST00000466561.1:n.1104C=
ENST00000502418.1:c.818C=	ENSP00000423065.1:p.Thr273=
NM_001141973.2:c.3215C=	NP_001135445.1:p.Thr1072=
NM_001141974.2:c.3098C=	NP_001135446.1:p.Thr1033=
NM_022089.3:c.3230C=	NP_071372.1:p.Thr1077=
XM_005245809.1:c.3230C=	XP_005245866.1:p.Thr1077=
XM_005245810.1:c.3227C=	XP_005245867.1:p.Thr1076=
XM_005245811.1:c.3215C=	XP_005245868.1:p.Thr1072=
XM_005245812.1:c.3203C=	XP_005245869.1:p.Thr1068=
XM_005245813.1:c.3170C=	XP_005245870.1:p.Thr1057=
XM_005245815.1:c.3113C=	XP_005245872.1:p.Thr1038=
XM_006710512.1:c.3212C=	XP_006710575.1:p.Thr1071=
XM_006710513.1:c.3188C=	XP_006710576.1:p.Thr1063=
XM_011541128.1:c.3215C=	XP_011539430.1:p.Thr1072=
XM_011541129.1:c.3023C=	XP_011539431.1:p.Thr1008=
XM_017000844.1:c.3215C=	XP_016856333.1:p.Thr1072=
XM_017000845.1:c.3212C=	XP_016856334.1:p.Thr1071=
XM_017000846.1:c.3188C=	XP_016856335.1:p.Thr1063=
XM_017000847.1:c.3185C=	XP_016856336.1:p.Thr1062=
XM_017000848.1:c.3113C=	XP_016856337.1:p.Thr1038=
XM_017000849.1:c.3098C=	XP_016856338.1:p.Thr1033=
XM_017000850.1:c.3023C=	XP_016856339.1:p.Thr1008=
NM_022089.4:c.3230C= MANE Select	NP_071372.1:p.Thr1077=
NM_001141973.3:c.3215C=	NP_001135445.1:p.Thr1072=
NM_001141974.3:c.3098C=	NP_001135446.1:p.Thr1033=