Canonical Allele Identifier: CA338233505

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17313357T>A (hg19) ; chr1:g.16986862T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986862T>A , CM000663.2:g.16986862T>A	GRCh38
NC_000001.10:g.17313357T>A , CM000663.1:g.17313357T>A	GRCh37
NC_000001.9:g.17185944T>A	NCBI36
NG_009054.1:g.30067A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3178A>T MANE Select	ENSP00000327214.8:p.Ile1060Phe
ENST00000326735.12:c.3178A>T	ENSP00000327214.8:p.Ile1060Phe
ENST00000341676.9:c.3046A>T	ENSP00000341115.5:p.Ile1016Phe
ENST00000452699.5:c.3163A>T	ENSP00000413307.1:p.Ile1055Phe
ENST00000466561.1:n.1052A>T
ENST00000502418.1:c.766A>T	ENSP00000423065.1:p.Ile256Phe
NM_001141973.2:c.3163A>T	NP_001135445.1:p.Ile1055Phe
NM_001141974.2:c.3046A>T	NP_001135446.1:p.Ile1016Phe
NM_022089.3:c.3178A>T	NP_071372.1:p.Ile1060Phe
XM_005245809.1:c.3178A>T	XP_005245866.1:p.Ile1060Phe
XM_005245810.1:c.3175A>T	XP_005245867.1:p.Ile1059Phe
XM_005245811.1:c.3163A>T	XP_005245868.1:p.Ile1055Phe
XM_005245812.1:c.3151A>T	XP_005245869.1:p.Ile1051Phe
XM_005245813.1:c.3118A>T	XP_005245870.1:p.Ile1040Phe
XM_005245815.1:c.3061A>T	XP_005245872.1:p.Ile1021Phe
XM_006710512.1:c.3160A>T	XP_006710575.1:p.Ile1054Phe
XM_006710513.1:c.3136A>T	XP_006710576.1:p.Ile1046Phe
XM_011541128.1:c.3163A>T	XP_011539430.1:p.Ile1055Phe
XM_011541129.1:c.2971A>T	XP_011539431.1:p.Ile991Phe
XM_017000844.1:c.3163A>T	XP_016856333.1:p.Ile1055Phe
XM_017000845.1:c.3160A>T	XP_016856334.1:p.Ile1054Phe
XM_017000846.1:c.3136A>T	XP_016856335.1:p.Ile1046Phe
XM_017000847.1:c.3133A>T	XP_016856336.1:p.Ile1045Phe
XM_017000848.1:c.3061A>T	XP_016856337.1:p.Ile1021Phe
XM_017000849.1:c.3046A>T	XP_016856338.1:p.Ile1016Phe
XM_017000850.1:c.2971A>T	XP_016856339.1:p.Ile991Phe
NM_022089.4:c.3178A>T MANE Select	NP_071372.1:p.Ile1060Phe
NM_001141973.3:c.3163A>T	NP_001135445.1:p.Ile1055Phe
NM_001141974.3:c.3046A>T	NP_001135446.1:p.Ile1016Phe