Canonical Allele Identifier: CA338232183

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312761C>T (hg19) ; chr1:g.16986266C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986266C>T , CM000663.2:g.16986266C>T	GRCh38
NC_000001.10:g.17312761C>T , CM000663.1:g.17312761C>T	GRCh37
NC_000001.9:g.17185348C>T	NCBI36
NG_009054.1:g.30663G>A
NG_029688.1:g.321G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3498G>A MANE Select	ENSP00000327214.8:p.Leu1166=
ENST00000326735.12:c.3498G>A	ENSP00000327214.8:p.Leu1166=
ENST00000341676.9:c.3196G>A	ENSP00000341115.5:p.Gly1066Ser
ENST00000452699.5:c.3483G>A	ENSP00000413307.1:p.Leu1161=
ENST00000466561.1:n.1544G>A
ENST00000502418.1:c.916G>A	ENSP00000423065.1:p.Gly306Ser
NM_001141973.2:c.3483G>A	NP_001135445.1:p.Leu1161=
NM_001141974.2:c.3196G>A	NP_001135446.1:p.Gly1066Ser
NM_022089.3:c.3498G>A	NP_071372.1:p.Leu1166=
XM_005245809.1:c.3328G>A	XP_005245866.1:p.Gly1110Ser
XM_005245810.1:c.3325G>A	XP_005245867.1:p.Gly1109Ser
XM_005245811.1:c.3313G>A	XP_005245868.1:p.Gly1105Ser
XM_005245812.1:c.3301G>A	XP_005245869.1:p.Gly1101Ser
XM_005245813.1:c.3268G>A	XP_005245870.1:p.Gly1090Ser
XM_005245815.1:c.3211G>A	XP_005245872.1:p.Gly1071Ser
XM_006710512.1:c.3310G>A	XP_006710575.1:p.Gly1104Ser
XM_006710513.1:c.3286G>A	XP_006710576.1:p.Gly1096Ser
XM_011541128.1:c.3313G>A	XP_011539430.1:p.Gly1105Ser
XM_011541129.1:c.3121G>A	XP_011539431.1:p.Gly1041Ser
XM_017000844.1:c.3483G>A	XP_016856333.1:p.Leu1161=
XM_017000845.1:c.3480G>A	XP_016856334.1:p.Leu1160=
XM_017000846.1:c.3456G>A	XP_016856335.1:p.Leu1152=
XM_017000847.1:c.3453G>A	XP_016856336.1:p.Leu1151=
XM_017000848.1:c.3381G>A	XP_016856337.1:p.Leu1127=
XM_017000849.1:c.3366G>A	XP_016856338.1:p.Leu1122=
XM_017000850.1:c.3291G>A	XP_016856339.1:p.Leu1097=
NM_022089.4:c.3498G>A MANE Select	NP_071372.1:p.Leu1166=
NM_001141973.3:c.3483G>A	NP_001135445.1:p.Leu1161=
NM_001141974.3:c.3196G>A	NP_001135446.1:p.Gly1066Ser