Canonical Allele Identifier: CA338232075

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312744G>C (hg19) ; chr1:g.16986249G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986249G>C , CM000663.2:g.16986249G>C	GRCh38
NC_000001.10:g.17312744G>C , CM000663.1:g.17312744G>C	GRCh37
NC_000001.9:g.17185331G>C	NCBI36
NG_009054.1:g.30680C>G
NG_029688.1:g.338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3515C>G MANE Select	ENSP00000327214.8:p.Pro1172Arg
ENST00000326735.12:c.3515C>G	ENSP00000327214.8:p.Pro1172Arg
ENST00000341676.9:c.3213C>G	ENSP00000341115.5:p.Ala1071=
ENST00000452699.5:c.3500C>G	ENSP00000413307.1:p.Pro1167Arg
ENST00000466561.1:n.1561C>G
ENST00000502418.1:c.933C>G	ENSP00000423065.1:p.Ala311=
NM_001141973.2:c.3500C>G	NP_001135445.1:p.Pro1167Arg
NM_001141974.2:c.3213C>G	NP_001135446.1:p.Ala1071=
NM_022089.3:c.3515C>G	NP_071372.1:p.Pro1172Arg
XM_005245809.1:c.3345C>G	XP_005245866.1:p.Ala1115=
XM_005245810.1:c.3342C>G	XP_005245867.1:p.Ala1114=
XM_005245811.1:c.3330C>G	XP_005245868.1:p.Ala1110=
XM_005245812.1:c.3318C>G	XP_005245869.1:p.Ala1106=
XM_005245813.1:c.3285C>G	XP_005245870.1:p.Ala1095=
XM_005245815.1:c.3228C>G	XP_005245872.1:p.Ala1076=
XM_006710512.1:c.3327C>G	XP_006710575.1:p.Ala1109=
XM_006710513.1:c.3303C>G	XP_006710576.1:p.Ala1101=
XM_011541128.1:c.3330C>G	XP_011539430.1:p.Ala1110=
XM_011541129.1:c.3138C>G	XP_011539431.1:p.Ala1046=
XM_017000844.1:c.3500C>G	XP_016856333.1:p.Pro1167Arg
XM_017000845.1:c.3497C>G	XP_016856334.1:p.Pro1166Arg
XM_017000846.1:c.3473C>G	XP_016856335.1:p.Pro1158Arg
XM_017000847.1:c.3470C>G	XP_016856336.1:p.Pro1157Arg
XM_017000848.1:c.3398C>G	XP_016856337.1:p.Pro1133Arg
XM_017000849.1:c.3383C>G	XP_016856338.1:p.Pro1128Arg
XM_017000850.1:c.3308C>G	XP_016856339.1:p.Pro1103Arg
NM_022089.4:c.3515C>G MANE Select	NP_071372.1:p.Pro1172Arg
NM_001141973.3:c.3500C>G	NP_001135445.1:p.Pro1167Arg
NM_001141974.3:c.3213C>G	NP_001135446.1:p.Ala1071=