Canonical Allele Identifier: CA338251580

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17322475T>A (hg19) ; chr1:g.16995980T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16995980T>A , CM000663.2:g.16995980T>A	GRCh38
NC_000001.10:g.17322475T>A , CM000663.1:g.17322475T>A	GRCh37
NC_000001.9:g.17195062T>A	NCBI36
NG_009054.1:g.20949A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1538A>T MANE Select	ENSP00000327214.8:p.Asp513Val
ENST00000326735.12:c.1538A>T	ENSP00000327214.8:p.Asp513Val
ENST00000341676.9:c.1523A>T	ENSP00000341115.5:p.Asp508Val
ENST00000452699.5:c.1523A>T	ENSP00000413307.1:p.Asp508Val
ENST00000463860.5:n.1146A>T
ENST00000502860.1:n.566A>T
ENST00000503552.1:c.215A>T	ENSP00000421126.1:p.Asp72Val
ENST00000617114.4:c.566A>T	ENSP00000478781.1:p.Asp189Val
NM_001141973.2:c.1523A>T	NP_001135445.1:p.Asp508Val
NM_001141974.2:c.1523A>T	NP_001135446.1:p.Asp508Val
NM_022089.3:c.1538A>T	NP_071372.1:p.Asp513Val
XM_005245809.1:c.1538A>T	XP_005245866.1:p.Asp513Val
XM_005245810.1:c.1535A>T	XP_005245867.1:p.Asp512Val
XM_005245811.1:c.1523A>T	XP_005245868.1:p.Asp508Val
XM_005245812.1:c.1511A>T	XP_005245869.1:p.Asp504Val
XM_005245813.1:c.1538A>T	XP_005245870.1:p.Asp513Val
XM_005245815.1:c.1538A>T	XP_005245872.1:p.Asp513Val
XM_006710512.1:c.1520A>T	XP_006710575.1:p.Asp507Val
XM_006710513.1:c.1496A>T	XP_006710576.1:p.Asp499Val
XM_011541128.1:c.1527+11A>T	XP_011539430.1:n.1527+11A>T
XM_011541129.1:c.1538A>T	XP_011539431.1:p.Asp513Val
XM_017000844.1:c.1527+11A>T	XP_016856333.1:n.1527+11A>T
XM_017000845.1:c.1520A>T	XP_016856334.1:p.Asp507Val
XM_017000846.1:c.1496A>T	XP_016856335.1:p.Asp499Val
XM_017000847.1:c.1497+11A>T	XP_016856336.1:n.1497+11A>T
XM_017000848.1:c.1538A>T	XP_016856337.1:p.Asp513Val
XM_017000849.1:c.1523A>T	XP_016856338.1:p.Asp508Val
XM_017000850.1:c.1538A>T	XP_016856339.1:p.Asp513Val
NM_022089.4:c.1538A>T MANE Select	NP_071372.1:p.Asp513Val
NM_001141973.3:c.1523A>T	NP_001135445.1:p.Asp508Val
NM_001141974.3:c.1523A>T	NP_001135446.1:p.Asp508Val