Canonical Allele Identifier: CA2742637222

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16995965_16995966del , CM000663.2:g.16995965_16995966del	GRCh38
NC_000001.10:g.17322460_17322461del , CM000663.1:g.17322460_17322461del	GRCh37
NC_000001.9:g.17195047_17195048del	NCBI36
NG_009054.1:g.20963_20964del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1542+10_1542+11del MANE Select	ENSP00000327214.8:n.1542+10_1542+11del
ENST00000326735.12:c.1542+10_1542+11del	ENSP00000327214.8:n.1542+10_1542+11del
ENST00000341676.9:c.1527+10_1527+11del	ENSP00000341115.5:n.1527+10_1527+11del
ENST00000452699.5:c.1527+10_1527+11del	ENSP00000413307.1:n.1527+10_1527+11del
ENST00000463860.5:n.1160_1161del
ENST00000502860.1:n.580_581del
ENST00000503552.1:c.219+10_219+11del	ENSP00000421126.1:n.219+10_219+11del
ENST00000617114.4:c.580_581del	ENSP00000478781.1:p.Gln194GlyfsTer?
NM_001141973.2:c.1527+10_1527+11del	NP_001135445.1:n.1527+10_1527+11del
NM_001141974.2:c.1527+10_1527+11del	NP_001135446.1:n.1527+10_1527+11del
NM_022089.3:c.1542+10_1542+11del	NP_071372.1:n.1542+10_1542+11del
XM_005245809.1:c.1542+10_1542+11del	XP_005245866.1:n.1542+10_1542+11del
XM_005245810.1:c.1539+10_1539+11del	XP_005245867.1:n.1539+10_1539+11del
XM_005245811.1:c.1527+10_1527+11del	XP_005245868.1:n.1527+10_1527+11del
XM_005245812.1:c.1515+10_1515+11del	XP_005245869.1:n.1515+10_1515+11del
XM_005245813.1:c.1542+10_1542+11del	XP_005245870.1:n.1542+10_1542+11del
XM_005245815.1:c.1542+10_1542+11del	XP_005245872.1:n.1542+10_1542+11del
XM_006710512.1:c.1524+10_1524+11del	XP_006710575.1:n.1524+10_1524+11del
XM_006710513.1:c.1500+10_1500+11del	XP_006710576.1:n.1500+10_1500+11del
XM_011541128.1:c.1527+25_1527+26del	XP_011539430.1:n.1527+25_1527+26del
XM_011541129.1:c.1542+10_1542+11del	XP_011539431.1:n.1542+10_1542+11del
XM_017000844.1:c.1527+25_1527+26del	XP_016856333.1:n.1527+25_1527+26del
XM_017000845.1:c.1524+10_1524+11del	XP_016856334.1:n.1524+10_1524+11del
XM_017000846.1:c.1500+10_1500+11del	XP_016856335.1:n.1500+10_1500+11del
XM_017000847.1:c.1497+25_1497+26del	XP_016856336.1:n.1497+25_1497+26del
XM_017000848.1:c.1542+10_1542+11del	XP_016856337.1:n.1542+10_1542+11del
XM_017000849.1:c.1527+10_1527+11del	XP_016856338.1:n.1527+10_1527+11del
XM_017000850.1:c.1542+10_1542+11del	XP_016856339.1:n.1542+10_1542+11del
NM_022089.4:c.1542+10_1542+11del MANE Select	NP_071372.1:n.1542+10_1542+11del
NM_001141973.3:c.1527+10_1527+11del	NP_001135445.1:n.1527+10_1527+11del
NM_001141974.3:c.1527+10_1527+11del	NP_001135446.1:n.1527+10_1527+11del