Canonical Allele Identifier: CA338253387

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17322790G>C (hg19) ; chr1:g.16996295G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16996295G>C , CM000663.2:g.16996295G>C	GRCh38
NC_000001.10:g.17322790G>C , CM000663.1:g.17322790G>C	GRCh37
NC_000001.9:g.17195377G>C	NCBI36
NG_009054.1:g.20634C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1312C>G MANE Select	ENSP00000327214.8:p.Leu438Val
ENST00000326735.12:c.1312C>G	ENSP00000327214.8:p.Leu438Val
ENST00000341676.9:c.1297C>G	ENSP00000341115.5:p.Leu433Val
ENST00000452699.5:c.1297C>G	ENSP00000413307.1:p.Leu433Val
ENST00000463860.5:n.920C>G
ENST00000502860.1:n.340C>G
ENST00000506174.5:c.454C>G	ENSP00000424393.1:p.Leu152Val
ENST00000509392.1:n.400C>G
ENST00000617114.4:c.340C>G	ENSP00000478781.1:p.Leu114Val
NM_001141973.2:c.1297C>G	NP_001135445.1:p.Leu433Val
NM_001141974.2:c.1297C>G	NP_001135446.1:p.Leu433Val
NM_022089.3:c.1312C>G	NP_071372.1:p.Leu438Val
XM_005245809.1:c.1312C>G	XP_005245866.1:p.Leu438Val
XM_005245810.1:c.1309C>G	XP_005245867.1:p.Leu437Val
XM_005245811.1:c.1297C>G	XP_005245868.1:p.Leu433Val
XM_005245812.1:c.1285C>G	XP_005245869.1:p.Leu429Val
XM_005245813.1:c.1312C>G	XP_005245870.1:p.Leu438Val
XM_005245815.1:c.1312C>G	XP_005245872.1:p.Leu438Val
XM_006710512.1:c.1294C>G	XP_006710575.1:p.Leu432Val
XM_006710513.1:c.1270C>G	XP_006710576.1:p.Leu424Val
XM_011541128.1:c.1312C>G	XP_011539430.1:p.Leu438Val
XM_011541129.1:c.1312C>G	XP_011539431.1:p.Leu438Val
XM_017000844.1:c.1312C>G	XP_016856333.1:p.Leu438Val
XM_017000845.1:c.1294C>G	XP_016856334.1:p.Leu432Val
XM_017000846.1:c.1270C>G	XP_016856335.1:p.Leu424Val
XM_017000847.1:c.1282C>G	XP_016856336.1:p.Leu428Val
XM_017000848.1:c.1312C>G	XP_016856337.1:p.Leu438Val
XM_017000849.1:c.1297C>G	XP_016856338.1:p.Leu433Val
XM_017000850.1:c.1312C>G	XP_016856339.1:p.Leu438Val
NM_022089.4:c.1312C>G MANE Select	NP_071372.1:p.Leu438Val
NM_001141973.3:c.1297C>G	NP_001135445.1:p.Leu433Val
NM_001141974.3:c.1297C>G	NP_001135446.1:p.Leu433Val