Canonical Allele Identifier: CA338233641

Gene: ATP13A2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986894A>C , CM000663.2:g.16986894A>C	GRCh38
NC_000001.10:g.17313389A>C , CM000663.1:g.17313389A>C	GRCh37
NC_000001.9:g.17185976A>C	NCBI36
NG_009054.1:g.30035T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3146T>G MANE Select	ENSP00000327214.8:p.Val1049Gly
ENST00000326735.12:c.3146T>G	ENSP00000327214.8:p.Val1049Gly
ENST00000341676.9:c.3014T>G	ENSP00000341115.5:p.Val1005Gly
ENST00000452699.5:c.3131T>G	ENSP00000413307.1:p.Val1044Gly
ENST00000466561.1:n.1020T>G
ENST00000502418.1:c.734T>G	ENSP00000423065.1:p.Val245Gly
NM_001141973.2:c.3131T>G	NP_001135445.1:p.Val1044Gly
NM_001141974.2:c.3014T>G	NP_001135446.1:p.Val1005Gly
NM_022089.3:c.3146T>G	NP_071372.1:p.Val1049Gly
XM_005245809.1:c.3146T>G	XP_005245866.1:p.Val1049Gly
XM_005245810.1:c.3143T>G	XP_005245867.1:p.Val1048Gly
XM_005245811.1:c.3131T>G	XP_005245868.1:p.Val1044Gly
XM_005245812.1:c.3119T>G	XP_005245869.1:p.Val1040Gly
XM_005245813.1:c.3086T>G	XP_005245870.1:p.Val1029Gly
XM_005245815.1:c.3029T>G	XP_005245872.1:p.Val1010Gly
XM_006710512.1:c.3128T>G	XP_006710575.1:p.Val1043Gly
XM_006710513.1:c.3104T>G	XP_006710576.1:p.Val1035Gly
XM_011541128.1:c.3131T>G	XP_011539430.1:p.Val1044Gly
XM_011541129.1:c.2939T>G	XP_011539431.1:p.Val980Gly
XM_017000844.1:c.3131T>G	XP_016856333.1:p.Val1044Gly
XM_017000845.1:c.3128T>G	XP_016856334.1:p.Val1043Gly
XM_017000846.1:c.3104T>G	XP_016856335.1:p.Val1035Gly
XM_017000847.1:c.3101T>G	XP_016856336.1:p.Val1034Gly
XM_017000848.1:c.3029T>G	XP_016856337.1:p.Val1010Gly
XM_017000849.1:c.3014T>G	XP_016856338.1:p.Val1005Gly
XM_017000850.1:c.2939T>G	XP_016856339.1:p.Val980Gly
NM_022089.4:c.3146T>G MANE Select	NP_071372.1:p.Val1049Gly
NM_001141973.3:c.3131T>G	NP_001135445.1:p.Val1044Gly
NM_001141974.3:c.3014T>G	NP_001135446.1:p.Val1005Gly