Canonical Allele Identifier: CA338252475

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17322586G>T (hg19) ; chr1:g.16996091G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16996091G>T , CM000663.2:g.16996091G>T	GRCh38
NC_000001.10:g.17322586G>T , CM000663.1:g.17322586G>T	GRCh37
NC_000001.9:g.17195173G>T	NCBI36
NG_009054.1:g.20838C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1427C>A MANE Select	ENSP00000327214.8:p.Ala476Asp
ENST00000326735.12:c.1427C>A	ENSP00000327214.8:p.Ala476Asp
ENST00000341676.9:c.1412C>A	ENSP00000341115.5:p.Ala471Asp
ENST00000452699.5:c.1412C>A	ENSP00000413307.1:p.Ala471Asp
ENST00000463860.5:n.1035C>A
ENST00000502860.1:n.455C>A
ENST00000503552.1:c.104C>A	ENSP00000421126.1:p.Ala35Asp
ENST00000506174.5:c.569C>A	ENSP00000424393.1:p.Ala190Asp
ENST00000509392.1:n.515C>A
ENST00000617114.4:c.455C>A	ENSP00000478781.1:p.Ala152Asp
NM_001141973.2:c.1412C>A	NP_001135445.1:p.Ala471Asp
NM_001141974.2:c.1412C>A	NP_001135446.1:p.Ala471Asp
NM_022089.3:c.1427C>A	NP_071372.1:p.Ala476Asp
XM_005245809.1:c.1427C>A	XP_005245866.1:p.Ala476Asp
XM_005245810.1:c.1424C>A	XP_005245867.1:p.Ala475Asp
XM_005245811.1:c.1412C>A	XP_005245868.1:p.Ala471Asp
XM_005245812.1:c.1400C>A	XP_005245869.1:p.Ala467Asp
XM_005245813.1:c.1427C>A	XP_005245870.1:p.Ala476Asp
XM_005245815.1:c.1427C>A	XP_005245872.1:p.Ala476Asp
XM_006710512.1:c.1409C>A	XP_006710575.1:p.Ala470Asp
XM_006710513.1:c.1385C>A	XP_006710576.1:p.Ala462Asp
XM_011541128.1:c.1427C>A	XP_011539430.1:p.Ala476Asp
XM_011541129.1:c.1427C>A	XP_011539431.1:p.Ala476Asp
XM_017000844.1:c.1427C>A	XP_016856333.1:p.Ala476Asp
XM_017000845.1:c.1409C>A	XP_016856334.1:p.Ala470Asp
XM_017000846.1:c.1385C>A	XP_016856335.1:p.Ala462Asp
XM_017000847.1:c.1397C>A	XP_016856336.1:p.Ala466Asp
XM_017000848.1:c.1427C>A	XP_016856337.1:p.Ala476Asp
XM_017000849.1:c.1412C>A	XP_016856338.1:p.Ala471Asp
XM_017000850.1:c.1427C>A	XP_016856339.1:p.Ala476Asp
NM_022089.4:c.1427C>A MANE Select	NP_071372.1:p.Ala476Asp
NM_001141973.3:c.1412C>A	NP_001135445.1:p.Ala471Asp
NM_001141974.3:c.1412C>A	NP_001135446.1:p.Ala471Asp