Canonical Allele Identifier: CA636538

Gene: ATP13A2

Linked Data

• ClinVar Variation Id: 2921503
• ClinVar RCV Id: RCV003780085
• dbSNP Id: rs761814059
• ExAC: 1:17313107 C / T
• gnomAD v2: 1-17313107-C-T
• gnomAD v3: 1-16986612-C-T
• gnomAD v4: 1-16986612-C-T
• MyVariant Identifiers: chr1:g.17313107C>T (hg19) ; chr1:g.16986612C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986612C>T , CM000663.2:g.16986612C>T	GRCh38
NC_000001.10:g.17313107C>T , CM000663.1:g.17313107C>T	GRCh37
NC_000001.9:g.17185694C>T	NCBI36
NG_009054.1:g.30317G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3256G>A MANE Select	ENSP00000327214.8:p.Ala1086Thr
ENST00000326735.12:c.3256G>A	ENSP00000327214.8:p.Ala1086Thr
ENST00000341676.9:c.3103+193G>A	ENSP00000341115.5:n.3103+193G>A
ENST00000452699.5:c.3241G>A	ENSP00000413307.1:p.Ala1081Thr
ENST00000466561.1:n.1302G>A
ENST00000502418.1:c.823+193G>A	ENSP00000423065.1:n.823+193G>A
NM_001141973.2:c.3241G>A	NP_001135445.1:p.Ala1081Thr
NM_001141974.2:c.3103+193G>A	NP_001135446.1:n.3103+193G>A
NM_022089.3:c.3256G>A	NP_071372.1:p.Ala1086Thr
XM_005245809.1:c.3235+193G>A	XP_005245866.1:n.3235+193G>A
XM_005245810.1:c.3232+193G>A	XP_005245867.1:n.3232+193G>A
XM_005245811.1:c.3220+193G>A	XP_005245868.1:n.3220+193G>A
XM_005245812.1:c.3208+193G>A	XP_005245869.1:n.3208+193G>A
XM_005245813.1:c.3175+193G>A	XP_005245870.1:n.3175+193G>A
XM_005245815.1:c.3118+193G>A	XP_005245872.1:n.3118+193G>A
XM_006710512.1:c.3217+193G>A	XP_006710575.1:n.3217+193G>A
XM_006710513.1:c.3193+193G>A	XP_006710576.1:n.3193+193G>A
XM_011541128.1:c.3220+193G>A	XP_011539430.1:n.3220+193G>A
XM_011541129.1:c.3028+193G>A	XP_011539431.1:n.3028+193G>A
XM_017000844.1:c.3241G>A	XP_016856333.1:p.Ala1081Thr
XM_017000845.1:c.3238G>A	XP_016856334.1:p.Ala1080Thr
XM_017000846.1:c.3214G>A	XP_016856335.1:p.Ala1072Thr
XM_017000847.1:c.3211G>A	XP_016856336.1:p.Ala1071Thr
XM_017000848.1:c.3139G>A	XP_016856337.1:p.Ala1047Thr
XM_017000849.1:c.3124G>A	XP_016856338.1:p.Ala1042Thr
XM_017000850.1:c.3049G>A	XP_016856339.1:p.Ala1017Thr
NM_022089.4:c.3256G>A MANE Select	NP_071372.1:p.Ala1086Thr
NM_001141973.3:c.3241G>A	NP_001135445.1:p.Ala1081Thr
NM_001141974.3:c.3103+193G>A	NP_001135446.1:n.3103+193G>A