Canonical Allele Identifier: CA338233409

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17313341A>C (hg19) ; chr1:g.16986846A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986846A>C , CM000663.2:g.16986846A>C	GRCh38
NC_000001.10:g.17313341A>C , CM000663.1:g.17313341A>C	GRCh37
NC_000001.9:g.17185928A>C	NCBI36
NG_009054.1:g.30083T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3194T>G MANE Select	ENSP00000327214.8:p.Val1065Gly
ENST00000326735.12:c.3194T>G	ENSP00000327214.8:p.Val1065Gly
ENST00000341676.9:c.3062T>G	ENSP00000341115.5:p.Val1021Gly
ENST00000452699.5:c.3179T>G	ENSP00000413307.1:p.Val1060Gly
ENST00000466561.1:n.1068T>G
ENST00000502418.1:c.782T>G	ENSP00000423065.1:p.Val261Gly
NM_001141973.2:c.3179T>G	NP_001135445.1:p.Val1060Gly
NM_001141974.2:c.3062T>G	NP_001135446.1:p.Val1021Gly
NM_022089.3:c.3194T>G	NP_071372.1:p.Val1065Gly
XM_005245809.1:c.3194T>G	XP_005245866.1:p.Val1065Gly
XM_005245810.1:c.3191T>G	XP_005245867.1:p.Val1064Gly
XM_005245811.1:c.3179T>G	XP_005245868.1:p.Val1060Gly
XM_005245812.1:c.3167T>G	XP_005245869.1:p.Val1056Gly
XM_005245813.1:c.3134T>G	XP_005245870.1:p.Val1045Gly
XM_005245815.1:c.3077T>G	XP_005245872.1:p.Val1026Gly
XM_006710512.1:c.3176T>G	XP_006710575.1:p.Val1059Gly
XM_006710513.1:c.3152T>G	XP_006710576.1:p.Val1051Gly
XM_011541128.1:c.3179T>G	XP_011539430.1:p.Val1060Gly
XM_011541129.1:c.2987T>G	XP_011539431.1:p.Val996Gly
XM_017000844.1:c.3179T>G	XP_016856333.1:p.Val1060Gly
XM_017000845.1:c.3176T>G	XP_016856334.1:p.Val1059Gly
XM_017000846.1:c.3152T>G	XP_016856335.1:p.Val1051Gly
XM_017000847.1:c.3149T>G	XP_016856336.1:p.Val1050Gly
XM_017000848.1:c.3077T>G	XP_016856337.1:p.Val1026Gly
XM_017000849.1:c.3062T>G	XP_016856338.1:p.Val1021Gly
XM_017000850.1:c.2987T>G	XP_016856339.1:p.Val996Gly
NM_022089.4:c.3194T>G MANE Select	NP_071372.1:p.Val1065Gly
NM_001141973.3:c.3179T>G	NP_001135445.1:p.Val1060Gly
NM_001141974.3:c.3062T>G	NP_001135446.1:p.Val1021Gly