Canonical Allele Identifier: CA338232410

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312805T>C (hg19) ; chr1:g.16986310T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986310T>C , CM000663.2:g.16986310T>C	GRCh38
NC_000001.10:g.17312805T>C , CM000663.1:g.17312805T>C	GRCh37
NC_000001.9:g.17185392T>C	NCBI36
NG_009054.1:g.30619A>G
NG_029688.1:g.277A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3454A>G MANE Select	ENSP00000327214.8:p.Lys1152Glu
ENST00000326735.12:c.3454A>G	ENSP00000327214.8:p.Lys1152Glu
ENST00000341676.9:c.3152A>G	ENSP00000341115.5:p.Gln1051Arg
ENST00000452699.5:c.3439A>G	ENSP00000413307.1:p.Lys1147Glu
ENST00000466561.1:n.1500A>G
ENST00000502418.1:c.872A>G	ENSP00000423065.1:p.Gln291Arg
NM_001141973.2:c.3439A>G	NP_001135445.1:p.Lys1147Glu
NM_001141974.2:c.3152A>G	NP_001135446.1:p.Gln1051Arg
NM_022089.3:c.3454A>G	NP_071372.1:p.Lys1152Glu
XM_005245809.1:c.3284A>G	XP_005245866.1:p.Gln1095Arg
XM_005245810.1:c.3281A>G	XP_005245867.1:p.Gln1094Arg
XM_005245811.1:c.3269A>G	XP_005245868.1:p.Gln1090Arg
XM_005245812.1:c.3257A>G	XP_005245869.1:p.Gln1086Arg
XM_005245813.1:c.3224A>G	XP_005245870.1:p.Gln1075Arg
XM_005245815.1:c.3167A>G	XP_005245872.1:p.Gln1056Arg
XM_006710512.1:c.3266A>G	XP_006710575.1:p.Gln1089Arg
XM_006710513.1:c.3242A>G	XP_006710576.1:p.Gln1081Arg
XM_011541128.1:c.3269A>G	XP_011539430.1:p.Gln1090Arg
XM_011541129.1:c.3077A>G	XP_011539431.1:p.Gln1026Arg
XM_017000844.1:c.3439A>G	XP_016856333.1:p.Lys1147Glu
XM_017000845.1:c.3436A>G	XP_016856334.1:p.Lys1146Glu
XM_017000846.1:c.3412A>G	XP_016856335.1:p.Lys1138Glu
XM_017000847.1:c.3409A>G	XP_016856336.1:p.Lys1137Glu
XM_017000848.1:c.3337A>G	XP_016856337.1:p.Lys1113Glu
XM_017000849.1:c.3322A>G	XP_016856338.1:p.Lys1108Glu
XM_017000850.1:c.3247A>G	XP_016856339.1:p.Lys1083Glu
NM_022089.4:c.3454A>G MANE Select	NP_071372.1:p.Lys1152Glu
NM_001141973.3:c.3439A>G	NP_001135445.1:p.Lys1147Glu
NM_001141974.3:c.3152A>G	NP_001135446.1:p.Gln1051Arg