Canonical Allele Identifier: CA1156021102

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989756G= , CM000663.2:g.16989756G=	GRCh38
NC_000001.10:g.17316251G= , CM000663.1:g.17316251G=	GRCh37
NC_000001.9:g.17188838G=	NCBI36
NG_009054.1:g.27173C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.2544C= MANE Select	ENSP00000327214.8:p.Gly848=
ENST00000326735.12:c.2544C=	ENSP00000327214.8:p.Gly848=
ENST00000341676.9:c.2412C=	ENSP00000341115.5:p.Gly804=
ENST00000452699.5:c.2529C=	ENSP00000413307.1:p.Gly843=
ENST00000466561.1:n.418C=
ENST00000502418.1:c.132C=	ENSP00000423065.1:p.Gly44=
NM_001141973.2:c.2529C=	NP_001135445.1:p.Gly843=
NM_001141974.2:c.2412C=	NP_001135446.1:p.Gly804=
NM_022089.3:c.2544C=	NP_071372.1:p.Gly848=
XM_005245809.1:c.2544C=	XP_005245866.1:p.Gly848=
XM_005245810.1:c.2541C=	XP_005245867.1:p.Gly847=
XM_005245811.1:c.2529C=	XP_005245868.1:p.Gly843=
XM_005245812.1:c.2517C=	XP_005245869.1:p.Gly839=
XM_005245813.1:c.2484C=	XP_005245870.1:p.Gly828=
XM_005245815.1:c.2427C=	XP_005245872.1:p.Gly809=
XM_006710512.1:c.2526C=	XP_006710575.1:p.Gly842=
XM_006710513.1:c.2502C=	XP_006710576.1:p.Gly834=
XM_011541128.1:c.2529C=	XP_011539430.1:p.Gly843=
XM_011541129.1:c.2337C=	XP_011539431.1:p.Gly779=
XM_017000844.1:c.2529C=	XP_016856333.1:p.Gly843=
XM_017000845.1:c.2526C=	XP_016856334.1:p.Gly842=
XM_017000846.1:c.2502C=	XP_016856335.1:p.Gly834=
XM_017000847.1:c.2499C=	XP_016856336.1:p.Gly833=
XM_017000848.1:c.2427C=	XP_016856337.1:p.Gly809=
XM_017000849.1:c.2412C=	XP_016856338.1:p.Gly804=
XM_017000850.1:c.2337C=	XP_016856339.1:p.Gly779=
NM_022089.4:c.2544C= MANE Select	NP_071372.1:p.Gly848=
NM_001141973.3:c.2529C=	NP_001135445.1:p.Gly843=
NM_001141974.3:c.2412C=	NP_001135446.1:p.Gly804=