Canonical Allele Identifier: CA338232297

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312782G>A (hg19) ; chr1:g.16986287G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986287G>A , CM000663.2:g.16986287G>A	GRCh38
NC_000001.10:g.17312782G>A , CM000663.1:g.17312782G>A	GRCh37
NC_000001.9:g.17185369G>A	NCBI36
NG_009054.1:g.30642C>T
NG_029688.1:g.300C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3477C>T MANE Select	ENSP00000327214.8:p.Phe1159=
ENST00000326735.12:c.3477C>T	ENSP00000327214.8:p.Phe1159=
ENST00000341676.9:c.3175C>T	ENSP00000341115.5:p.Gln1059Ter
ENST00000452699.5:c.3462C>T	ENSP00000413307.1:p.Phe1154=
ENST00000466561.1:n.1523C>T
ENST00000502418.1:c.895C>T	ENSP00000423065.1:p.Gln299Ter
NM_001141973.2:c.3462C>T	NP_001135445.1:p.Phe1154=
NM_001141974.2:c.3175C>T	NP_001135446.1:p.Gln1059Ter
NM_022089.3:c.3477C>T	NP_071372.1:p.Phe1159=
XM_005245809.1:c.3307C>T	XP_005245866.1:p.Gln1103Ter
XM_005245810.1:c.3304C>T	XP_005245867.1:p.Gln1102Ter
XM_005245811.1:c.3292C>T	XP_005245868.1:p.Gln1098Ter
XM_005245812.1:c.3280C>T	XP_005245869.1:p.Gln1094Ter
XM_005245813.1:c.3247C>T	XP_005245870.1:p.Gln1083Ter
XM_005245815.1:c.3190C>T	XP_005245872.1:p.Gln1064Ter
XM_006710512.1:c.3289C>T	XP_006710575.1:p.Gln1097Ter
XM_006710513.1:c.3265C>T	XP_006710576.1:p.Gln1089Ter
XM_011541128.1:c.3292C>T	XP_011539430.1:p.Gln1098Ter
XM_011541129.1:c.3100C>T	XP_011539431.1:p.Gln1034Ter
XM_017000844.1:c.3462C>T	XP_016856333.1:p.Phe1154=
XM_017000845.1:c.3459C>T	XP_016856334.1:p.Phe1153=
XM_017000846.1:c.3435C>T	XP_016856335.1:p.Phe1145=
XM_017000847.1:c.3432C>T	XP_016856336.1:p.Phe1144=
XM_017000848.1:c.3360C>T	XP_016856337.1:p.Phe1120=
XM_017000849.1:c.3345C>T	XP_016856338.1:p.Phe1115=
XM_017000850.1:c.3270C>T	XP_016856339.1:p.Phe1090=
NM_022089.4:c.3477C>T MANE Select	NP_071372.1:p.Phe1159=
NM_001141973.3:c.3462C>T	NP_001135445.1:p.Phe1154=
NM_001141974.3:c.3175C>T	NP_001135446.1:p.Gln1059Ter