Canonical Allele Identifier: CA416094129

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17316409C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989914C>A , CM000663.2:g.16989914C>A	GRCh38
NC_000001.10:g.17316409C>A , CM000663.1:g.17316409C>A	GRCh37
NC_000001.9:g.17188996C>A	NCBI36
NG_009054.1:g.27015G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.2502G>T MANE Select	ENSP00000327214.8:p.Val834=
ENST00000326735.12:c.2502G>T	ENSP00000327214.8:p.Val834=
ENST00000341676.9:c.2398-144G>T	ENSP00000341115.5:n.2398-144G>T
ENST00000452699.5:c.2487G>T	ENSP00000413307.1:p.Val829=
ENST00000466561.1:n.376G>T
ENST00000502418.1:c.90G>T	ENSP00000423065.1:p.Val30=
NM_001141973.2:c.2487G>T	NP_001135445.1:p.Val829=
NM_001141974.2:c.2398-144G>T	NP_001135446.1:n.2398-144G>T
NM_022089.3:c.2502G>T	NP_071372.1:p.Val834=
XM_005245809.1:c.2502G>T	XP_005245866.1:p.Val834=
XM_005245810.1:c.2499G>T	XP_005245867.1:p.Val833=
XM_005245811.1:c.2487G>T	XP_005245868.1:p.Val829=
XM_005245812.1:c.2475G>T	XP_005245869.1:p.Val825=
XM_005245813.1:c.2442G>T	XP_005245870.1:p.Val814=
XM_005245815.1:c.2413-144G>T	XP_005245872.1:n.2413-144G>T
XM_006710512.1:c.2484G>T	XP_006710575.1:p.Val828=
XM_006710513.1:c.2460G>T	XP_006710576.1:p.Val820=
XM_011541128.1:c.2487G>T	XP_011539430.1:p.Val829=
XM_011541129.1:c.2295G>T	XP_011539431.1:p.Val765=
XM_017000844.1:c.2487G>T	XP_016856333.1:p.Val829=
XM_017000845.1:c.2484G>T	XP_016856334.1:p.Val828=
XM_017000846.1:c.2460G>T	XP_016856335.1:p.Val820=
XM_017000847.1:c.2457G>T	XP_016856336.1:p.Val819=
XM_017000848.1:c.2413-144G>T	XP_016856337.1:n.2413-144G>T
XM_017000849.1:c.2398-144G>T	XP_016856338.1:n.2398-144G>T
XM_017000850.1:c.2295G>T	XP_016856339.1:p.Val765=
NM_022089.4:c.2502G>T MANE Select	NP_071372.1:p.Val834=
NM_001141973.3:c.2487G>T	NP_001135445.1:p.Val829=
NM_001141974.3:c.2398-144G>T	NP_001135446.1:n.2398-144G>T