Canonical Allele Identifier: CA636522

Gene: ATP13A2

Linked Data

• dbSNP Id: rs765405083
• ExAC: 1:17313030 G / T
• gnomAD v2: 1-17313030-G-T
• gnomAD v4: 1-16986535-G-T
• MyVariant Identifiers: chr1:g.17313030G>T (hg19) ; chr1:g.16986535G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986535G>T , CM000663.2:g.16986535G>T	GRCh38
NC_000001.10:g.17313030G>T , CM000663.1:g.17313030G>T	GRCh37
NC_000001.9:g.17185617G>T	NCBI36
NG_009054.1:g.30394C>A
NG_029688.1:g.52C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.3333C>A MANE Select	ENSP00000327214.8:p.Ile1111=
ENST00000326735.12:c.3333C>A	ENSP00000327214.8:p.Ile1111=
ENST00000341676.9:c.3104-177C>A	ENSP00000341115.5:n.3104-177C>A
ENST00000452699.5:c.3318C>A	ENSP00000413307.1:p.Ile1106=
ENST00000466561.1:n.1379C>A
ENST00000502418.1:c.824-177C>A	ENSP00000423065.1:n.824-177C>A
NM_001141973.2:c.3318C>A	NP_001135445.1:p.Ile1106=
NM_001141974.2:c.3104-177C>A	NP_001135446.1:n.3104-177C>A
NM_022089.3:c.3333C>A	NP_071372.1:p.Ile1111=
XM_005245809.1:c.3236-177C>A	XP_005245866.1:n.3236-177C>A
XM_005245810.1:c.3233-177C>A	XP_005245867.1:n.3233-177C>A
XM_005245811.1:c.3221-177C>A	XP_005245868.1:n.3221-177C>A
XM_005245812.1:c.3209-177C>A	XP_005245869.1:n.3209-177C>A
XM_005245813.1:c.3176-177C>A	XP_005245870.1:n.3176-177C>A
XM_005245815.1:c.3119-177C>A	XP_005245872.1:n.3119-177C>A
XM_006710512.1:c.3218-177C>A	XP_006710575.1:n.3218-177C>A
XM_006710513.1:c.3194-177C>A	XP_006710576.1:n.3194-177C>A
XM_011541128.1:c.3221-177C>A	XP_011539430.1:n.3221-177C>A
XM_011541129.1:c.3029-177C>A	XP_011539431.1:n.3029-177C>A
XM_017000844.1:c.3318C>A	XP_016856333.1:p.Ile1106=
XM_017000845.1:c.3315C>A	XP_016856334.1:p.Ile1105=
XM_017000846.1:c.3291C>A	XP_016856335.1:p.Ile1097=
XM_017000847.1:c.3288C>A	XP_016856336.1:p.Ile1096=
XM_017000848.1:c.3216C>A	XP_016856337.1:p.Ile1072=
XM_017000849.1:c.3201C>A	XP_016856338.1:p.Ile1067=
XM_017000850.1:c.3126C>A	XP_016856339.1:p.Ile1042=
NM_022089.4:c.3333C>A MANE Select	NP_071372.1:p.Ile1111=
NM_001141973.3:c.3318C>A	NP_001135445.1:p.Ile1106=
NM_001141974.3:c.3104-177C>A	NP_001135446.1:n.3104-177C>A