Canonical Allele Identifier: CA416093451

Gene: ATP13A2

Linked Data

• gnomAD v4: 1-16986236-G-T
• MyVariant Identifiers: chr1:g.17312731G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986236G>T , CM000663.2:g.16986236G>T	GRCh38
NC_000001.10:g.17312731G>T , CM000663.1:g.17312731G>T	GRCh37
NC_000001.9:g.17185318G>T	NCBI36
NG_009054.1:g.30693C>A
NG_029688.1:g.351C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3528C>A MANE Select	ENSP00000327214.8:p.Ala1176=
ENST00000326735.12:c.3528C>A	ENSP00000327214.8:p.Ala1176=
ENST00000341676.9:c.3226C>A	ENSP00000341115.5:p.Arg1076=
ENST00000452699.5:c.3513C>A	ENSP00000413307.1:p.Ala1171=
ENST00000466561.1:n.1574C>A
ENST00000502418.1:c.946C>A	ENSP00000423065.1:p.Arg316=
NM_001141973.2:c.3513C>A	NP_001135445.1:p.Ala1171=
NM_001141974.2:c.3226C>A	NP_001135446.1:p.Arg1076=
NM_022089.3:c.3528C>A	NP_071372.1:p.Ala1176=
XM_005245809.1:c.3358C>A	XP_005245866.1:p.Arg1120=
XM_005245810.1:c.3355C>A	XP_005245867.1:p.Arg1119=
XM_005245811.1:c.3343C>A	XP_005245868.1:p.Arg1115=
XM_005245812.1:c.3331C>A	XP_005245869.1:p.Arg1111=
XM_005245813.1:c.3298C>A	XP_005245870.1:p.Arg1100=
XM_005245815.1:c.3241C>A	XP_005245872.1:p.Arg1081=
XM_006710512.1:c.3340C>A	XP_006710575.1:p.Arg1114=
XM_006710513.1:c.3316C>A	XP_006710576.1:p.Arg1106=
XM_011541128.1:c.3343C>A	XP_011539430.1:p.Arg1115=
XM_011541129.1:c.3151C>A	XP_011539431.1:p.Arg1051=
XM_017000844.1:c.3513C>A	XP_016856333.1:p.Ala1171=
XM_017000845.1:c.3510C>A	XP_016856334.1:p.Ala1170=
XM_017000846.1:c.3486C>A	XP_016856335.1:p.Ala1162=
XM_017000847.1:c.3483C>A	XP_016856336.1:p.Ala1161=
XM_017000848.1:c.3411C>A	XP_016856337.1:p.Ala1137=
XM_017000849.1:c.3396C>A	XP_016856338.1:p.Ala1132=
XM_017000850.1:c.3321C>A	XP_016856339.1:p.Ala1107=
NM_022089.4:c.3528C>A MANE Select	NP_071372.1:p.Ala1176=
NM_001141973.3:c.3513C>A	NP_001135445.1:p.Ala1171=
NM_001141974.3:c.3226C>A	NP_001135446.1:p.Arg1076=