Canonical Allele Identifier: CA338233562

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17313370G>C (hg19) ; chr1:g.16986875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986875G>C , CM000663.2:g.16986875G>C	GRCh38
NC_000001.10:g.17313370G>C , CM000663.1:g.17313370G>C	GRCh37
NC_000001.9:g.17185957G>C	NCBI36
NG_009054.1:g.30054C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3165C>G MANE Select	ENSP00000327214.8:p.Ser1055Arg
ENST00000326735.12:c.3165C>G	ENSP00000327214.8:p.Ser1055Arg
ENST00000341676.9:c.3033C>G	ENSP00000341115.5:p.Ser1011Arg
ENST00000452699.5:c.3150C>G	ENSP00000413307.1:p.Ser1050Arg
ENST00000466561.1:n.1039C>G
ENST00000502418.1:c.753C>G	ENSP00000423065.1:p.Ser251Arg
NM_001141973.2:c.3150C>G	NP_001135445.1:p.Ser1050Arg
NM_001141974.2:c.3033C>G	NP_001135446.1:p.Ser1011Arg
NM_022089.3:c.3165C>G	NP_071372.1:p.Ser1055Arg
XM_005245809.1:c.3165C>G	XP_005245866.1:p.Ser1055Arg
XM_005245810.1:c.3162C>G	XP_005245867.1:p.Ser1054Arg
XM_005245811.1:c.3150C>G	XP_005245868.1:p.Ser1050Arg
XM_005245812.1:c.3138C>G	XP_005245869.1:p.Ser1046Arg
XM_005245813.1:c.3105C>G	XP_005245870.1:p.Ser1035Arg
XM_005245815.1:c.3048C>G	XP_005245872.1:p.Ser1016Arg
XM_006710512.1:c.3147C>G	XP_006710575.1:p.Ser1049Arg
XM_006710513.1:c.3123C>G	XP_006710576.1:p.Ser1041Arg
XM_011541128.1:c.3150C>G	XP_011539430.1:p.Ser1050Arg
XM_011541129.1:c.2958C>G	XP_011539431.1:p.Ser986Arg
XM_017000844.1:c.3150C>G	XP_016856333.1:p.Ser1050Arg
XM_017000845.1:c.3147C>G	XP_016856334.1:p.Ser1049Arg
XM_017000846.1:c.3123C>G	XP_016856335.1:p.Ser1041Arg
XM_017000847.1:c.3120C>G	XP_016856336.1:p.Ser1040Arg
XM_017000848.1:c.3048C>G	XP_016856337.1:p.Ser1016Arg
XM_017000849.1:c.3033C>G	XP_016856338.1:p.Ser1011Arg
XM_017000850.1:c.2958C>G	XP_016856339.1:p.Ser986Arg
NM_022089.4:c.3165C>G MANE Select	NP_071372.1:p.Ser1055Arg
NM_001141973.3:c.3150C>G	NP_001135445.1:p.Ser1050Arg
NM_001141974.3:c.3033C>G	NP_001135446.1:p.Ser1011Arg