Canonical Allele Identifier: CA1156050180

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986749_16986761delinsCCCCAGGGCTCCT , CM000663.2:g.16986749_16986761delinsCCCCAGGGCTCCT	GRCh38
NC_000001.10:g.17313244_17313256delinsCCCCAGGGCTCCT , CM000663.1:g.17313244_17313256delinsCCCCAGGGCTCCT	GRCh37
NC_000001.9:g.17185831_17185843delinsCCCCAGGGCTCCT	NCBI36
NG_009054.1:g.30168_30180delinsAGGAGCCCTGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.3235+44_3235+56delinsAGGAGCCCTGGGG MANE Select	ENSP00000327214.8:n.3235+44_3235+56delinsAGGAGCCCTGGGG
ENST00000326735.12:c.3235+44_3235+56delinsAGGAGCCCTGGGG	ENSP00000327214.8:n.3235+44_3235+56delinsAGGAGCCCTGGGG
ENST00000341676.9:c.3103+44_3103+56delinsAGGAGCCCTGGGG	ENSP00000341115.5:n.3103+44_3103+56delinsAGGAGCCCTGGGG
ENST00000452699.5:c.3220+44_3220+56delinsAGGAGCCCTGGGG	ENSP00000413307.1:n.3220+44_3220+56delinsAGGAGCCCTGGGG
ENST00000466561.1:n.1153_1165delinsAGGAGCCCTGGGG
ENST00000502418.1:c.823+44_823+56delinsAGGAGCCCTGGGG	ENSP00000423065.1:n.823+44_823+56delinsAGGAGCCCTGGGG
NM_001141973.2:c.3220+44_3220+56delinsAGGAGCCCTGGGG	NP_001135445.1:n.3220+44_3220+56delinsAGGAGCCCTGGGG
NM_001141974.2:c.3103+44_3103+56delinsAGGAGCCCTGGGG	NP_001135446.1:n.3103+44_3103+56delinsAGGAGCCCTGGGG
NM_022089.3:c.3235+44_3235+56delinsAGGAGCCCTGGGG	NP_071372.1:n.3235+44_3235+56delinsAGGAGCCCTGGGG
XM_005245809.1:c.3235+44_3235+56delinsAGGAGCCCTGGGG	XP_005245866.1:n.3235+44_3235+56delinsAGGAGCCCTGGGG
XM_005245810.1:c.3232+44_3232+56delinsAGGAGCCCTGGGG	XP_005245867.1:n.3232+44_3232+56delinsAGGAGCCCTGGGG
XM_005245811.1:c.3220+44_3220+56delinsAGGAGCCCTGGGG	XP_005245868.1:n.3220+44_3220+56delinsAGGAGCCCTGGGG
XM_005245812.1:c.3208+44_3208+56delinsAGGAGCCCTGGGG	XP_005245869.1:n.3208+44_3208+56delinsAGGAGCCCTGGGG
XM_005245813.1:c.3175+44_3175+56delinsAGGAGCCCTGGGG	XP_005245870.1:n.3175+44_3175+56delinsAGGAGCCCTGGGG
XM_005245815.1:c.3118+44_3118+56delinsAGGAGCCCTGGGG	XP_005245872.1:n.3118+44_3118+56delinsAGGAGCCCTGGGG
XM_006710512.1:c.3217+44_3217+56delinsAGGAGCCCTGGGG	XP_006710575.1:n.3217+44_3217+56delinsAGGAGCCCTGGGG
XM_006710513.1:c.3193+44_3193+56delinsAGGAGCCCTGGGG	XP_006710576.1:n.3193+44_3193+56delinsAGGAGCCCTGGGG
XM_011541128.1:c.3220+44_3220+56delinsAGGAGCCCTGGGG	XP_011539430.1:n.3220+44_3220+56delinsAGGAGCCCTGGGG
XM_011541129.1:c.3028+44_3028+56delinsAGGAGCCCTGGGG	XP_011539431.1:n.3028+44_3028+56delinsAGGAGCCCTGGGG
XM_017000844.1:c.3220+44_3220+56delinsAGGAGCCCTGGGG	XP_016856333.1:n.3220+44_3220+56delinsAGGAGCCCTGGGG
XM_017000845.1:c.3217+44_3217+56delinsAGGAGCCCTGGGG	XP_016856334.1:n.3217+44_3217+56delinsAGGAGCCCTGGGG
XM_017000846.1:c.3193+44_3193+56delinsAGGAGCCCTGGGG	XP_016856335.1:n.3193+44_3193+56delinsAGGAGCCCTGGGG
XM_017000847.1:c.3190+44_3190+56delinsAGGAGCCCTGGGG	XP_016856336.1:n.3190+44_3190+56delinsAGGAGCCCTGGGG
XM_017000848.1:c.3118+44_3118+56delinsAGGAGCCCTGGGG	XP_016856337.1:n.3118+44_3118+56delinsAGGAGCCCTGGGG
XM_017000849.1:c.3103+44_3103+56delinsAGGAGCCCTGGGG	XP_016856338.1:n.3103+44_3103+56delinsAGGAGCCCTGGGG
XM_017000850.1:c.3028+44_3028+56delinsAGGAGCCCTGGGG	XP_016856339.1:n.3028+44_3028+56delinsAGGAGCCCTGGGG
NM_022089.4:c.3235+44_3235+56delinsAGGAGCCCTGGGG MANE Select	NP_071372.1:n.3235+44_3235+56delinsAGGAGCCCTGGGG
NM_001141973.3:c.3220+44_3220+56delinsAGGAGCCCTGGGG	NP_001135445.1:n.3220+44_3220+56delinsAGGAGCCCTGGGG
NM_001141974.3:c.3103+44_3103+56delinsAGGAGCCCTGGGG	NP_001135446.1:n.3103+44_3103+56delinsAGGAGCCCTGGGG