Canonical Allele Identifier: CA416093542

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312970G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986475G>C , CM000663.2:g.16986475G>C	GRCh38
NC_000001.10:g.17312970G>C , CM000663.1:g.17312970G>C	GRCh37
NC_000001.9:g.17185557G>C	NCBI36
NG_009054.1:g.30454C>G
NG_029688.1:g.112C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3393C>G MANE Select	ENSP00000327214.8:p.Ala1131=
ENST00000326735.12:c.3393C>G	ENSP00000327214.8:p.Ala1131=
ENST00000341676.9:c.3104-117C>G	ENSP00000341115.5:n.3104-117C>G
ENST00000452699.5:c.3378C>G	ENSP00000413307.1:p.Ala1126=
ENST00000466561.1:n.1439C>G
ENST00000502418.1:c.824-117C>G	ENSP00000423065.1:n.824-117C>G
NM_001141973.2:c.3378C>G	NP_001135445.1:p.Ala1126=
NM_001141974.2:c.3104-117C>G	NP_001135446.1:n.3104-117C>G
NM_022089.3:c.3393C>G	NP_071372.1:p.Ala1131=
XM_005245809.1:c.3236-117C>G	XP_005245866.1:n.3236-117C>G
XM_005245810.1:c.3233-117C>G	XP_005245867.1:n.3233-117C>G
XM_005245811.1:c.3221-117C>G	XP_005245868.1:n.3221-117C>G
XM_005245812.1:c.3209-117C>G	XP_005245869.1:n.3209-117C>G
XM_005245813.1:c.3176-117C>G	XP_005245870.1:n.3176-117C>G
XM_005245815.1:c.3119-117C>G	XP_005245872.1:n.3119-117C>G
XM_006710512.1:c.3218-117C>G	XP_006710575.1:n.3218-117C>G
XM_006710513.1:c.3194-117C>G	XP_006710576.1:n.3194-117C>G
XM_011541128.1:c.3221-117C>G	XP_011539430.1:n.3221-117C>G
XM_011541129.1:c.3029-117C>G	XP_011539431.1:n.3029-117C>G
XM_017000844.1:c.3378C>G	XP_016856333.1:p.Ala1126=
XM_017000845.1:c.3375C>G	XP_016856334.1:p.Ala1125=
XM_017000846.1:c.3351C>G	XP_016856335.1:p.Ala1117=
XM_017000847.1:c.3348C>G	XP_016856336.1:p.Ala1116=
XM_017000848.1:c.3276C>G	XP_016856337.1:p.Ala1092=
XM_017000849.1:c.3261C>G	XP_016856338.1:p.Ala1087=
XM_017000850.1:c.3186C>G	XP_016856339.1:p.Ala1062=
NM_022089.4:c.3393C>G MANE Select	NP_071372.1:p.Ala1131=
NM_001141973.3:c.3378C>G	NP_001135445.1:p.Ala1126=
NM_001141974.3:c.3104-117C>G	NP_001135446.1:n.3104-117C>G