Canonical Allele Identifier: CA416093608

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17313355G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986860G>A , CM000663.2:g.16986860G>A	GRCh38
NC_000001.10:g.17313355G>A , CM000663.1:g.17313355G>A	GRCh37
NC_000001.9:g.17185942G>A	NCBI36
NG_009054.1:g.30069C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3180C>T MANE Select	ENSP00000327214.8:p.Ile1060=
ENST00000326735.12:c.3180C>T	ENSP00000327214.8:p.Ile1060=
ENST00000341676.9:c.3048C>T	ENSP00000341115.5:p.Ile1016=
ENST00000452699.5:c.3165C>T	ENSP00000413307.1:p.Ile1055=
ENST00000466561.1:n.1054C>T
ENST00000502418.1:c.768C>T	ENSP00000423065.1:p.Ile256=
NM_001141973.2:c.3165C>T	NP_001135445.1:p.Ile1055=
NM_001141974.2:c.3048C>T	NP_001135446.1:p.Ile1016=
NM_022089.3:c.3180C>T	NP_071372.1:p.Ile1060=
XM_005245809.1:c.3180C>T	XP_005245866.1:p.Ile1060=
XM_005245810.1:c.3177C>T	XP_005245867.1:p.Ile1059=
XM_005245811.1:c.3165C>T	XP_005245868.1:p.Ile1055=
XM_005245812.1:c.3153C>T	XP_005245869.1:p.Ile1051=
XM_005245813.1:c.3120C>T	XP_005245870.1:p.Ile1040=
XM_005245815.1:c.3063C>T	XP_005245872.1:p.Ile1021=
XM_006710512.1:c.3162C>T	XP_006710575.1:p.Ile1054=
XM_006710513.1:c.3138C>T	XP_006710576.1:p.Ile1046=
XM_011541128.1:c.3165C>T	XP_011539430.1:p.Ile1055=
XM_011541129.1:c.2973C>T	XP_011539431.1:p.Ile991=
XM_017000844.1:c.3165C>T	XP_016856333.1:p.Ile1055=
XM_017000845.1:c.3162C>T	XP_016856334.1:p.Ile1054=
XM_017000846.1:c.3138C>T	XP_016856335.1:p.Ile1046=
XM_017000847.1:c.3135C>T	XP_016856336.1:p.Ile1045=
XM_017000848.1:c.3063C>T	XP_016856337.1:p.Ile1021=
XM_017000849.1:c.3048C>T	XP_016856338.1:p.Ile1016=
XM_017000850.1:c.2973C>T	XP_016856339.1:p.Ile991=
NM_022089.4:c.3180C>T MANE Select	NP_071372.1:p.Ile1060=
NM_001141973.3:c.3165C>T	NP_001135445.1:p.Ile1055=
NM_001141974.3:c.3048C>T	NP_001135446.1:p.Ile1016=