Canonical Allele Identifier: CA1156029805

Gene: ATP13A2

Linked Data

• dbSNP Id: rs112882794

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16995747_16995749del , CM000663.2:g.16995747_16995749del	GRCh38
NC_000001.10:g.17322242_17322244del , CM000663.1:g.17322242_17322244del	GRCh37
NC_000001.9:g.17194829_17194831del	NCBI36
NG_009054.1:g.21183_21185del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1542+230_1542+232del MANE Select	ENSP00000327214.8:n.1542+230_1542+232del
ENST00000326735.12:c.1542+230_1542+232del	ENSP00000327214.8:n.1542+230_1542+232del
ENST00000341676.9:c.1527+230_1527+232del	ENSP00000341115.5:n.1527+230_1527+232del
ENST00000452699.5:c.1527+230_1527+232del	ENSP00000413307.1:n.1527+230_1527+232del
ENST00000463860.5:n.1380_1382del
ENST00000503552.1:c.219+230_219+232del	ENSP00000421126.1:n.219+230_219+232del
NM_001141973.2:c.1527+230_1527+232del	NP_001135445.1:n.1527+230_1527+232del
NM_001141974.2:c.1527+230_1527+232del	NP_001135446.1:n.1527+230_1527+232del
NM_022089.3:c.1542+230_1542+232del	NP_071372.1:n.1542+230_1542+232del
XM_005245809.1:c.1542+230_1542+232del	XP_005245866.1:n.1542+230_1542+232del
XM_005245810.1:c.1539+230_1539+232del	XP_005245867.1:n.1539+230_1539+232del
XM_005245811.1:c.1527+230_1527+232del	XP_005245868.1:n.1527+230_1527+232del
XM_005245812.1:c.1515+230_1515+232del	XP_005245869.1:n.1515+230_1515+232del
XM_005245813.1:c.1542+230_1542+232del	XP_005245870.1:n.1542+230_1542+232del
XM_005245815.1:c.1542+230_1542+232del	XP_005245872.1:n.1542+230_1542+232del
XM_006710512.1:c.1524+230_1524+232del	XP_006710575.1:n.1524+230_1524+232del
XM_006710513.1:c.1500+230_1500+232del	XP_006710576.1:n.1500+230_1500+232del
XM_011541128.1:c.1527+245_1527+247del	XP_011539430.1:n.1527+245_1527+247del
XM_011541129.1:c.1542+230_1542+232del	XP_011539431.1:n.1542+230_1542+232del
XM_017000844.1:c.1527+245_1527+247del	XP_016856333.1:n.1527+245_1527+247del
XM_017000845.1:c.1524+230_1524+232del	XP_016856334.1:n.1524+230_1524+232del
XM_017000846.1:c.1500+230_1500+232del	XP_016856335.1:n.1500+230_1500+232del
XM_017000847.1:c.1497+245_1497+247del	XP_016856336.1:n.1497+245_1497+247del
XM_017000848.1:c.1542+230_1542+232del	XP_016856337.1:n.1542+230_1542+232del
XM_017000849.1:c.1527+230_1527+232del	XP_016856338.1:n.1527+230_1527+232del
XM_017000850.1:c.1542+230_1542+232del	XP_016856339.1:n.1542+230_1542+232del
NM_022089.4:c.1542+230_1542+232del MANE Select	NP_071372.1:n.1542+230_1542+232del
NM_001141973.3:c.1527+230_1527+232del	NP_001135445.1:n.1527+230_1527+232del
NM_001141974.3:c.1527+230_1527+232del	NP_001135446.1:n.1527+230_1527+232del