Canonical Allele Identifier: CA338230490

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312530G>C (hg19) ; chr1:g.16986035G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986035G>C , CM000663.2:g.16986035G>C	GRCh38
NC_000001.10:g.17312530G>C , CM000663.1:g.17312530G>C	GRCh37
NC_000001.9:g.17185117G>C	NCBI36
NG_009054.1:g.30894C>G
NG_029688.1:g.552C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.*186C>G MANE Select	ENSP00000327214.8:n.*186C>G
ENST00000326735.12:c.*186C>G	ENSP00000327214.8:n.*186C>G
ENST00000341676.9:c.3427C>G	ENSP00000341115.5:p.Pro1143Ala
ENST00000452699.5:c.*186C>G	ENSP00000413307.1:n.*186C>G
ENST00000466561.1:n.1775C>G
ENST00000502418.1:c.1147C>G	ENSP00000423065.1:p.Pro383Ala
NM_001141973.2:c.*186C>G	NP_001135445.1:n.*186C>G
NM_001141974.2:c.3427C>G	NP_001135446.1:p.Pro1143Ala
NM_022089.3:c.*186C>G	NP_071372.1:n.*186C>G
XM_005245809.1:c.3559C>G	XP_005245866.1:p.Pro1187Ala
XM_005245810.1:c.3556C>G	XP_005245867.1:p.Pro1186Ala
XM_005245811.1:c.3544C>G	XP_005245868.1:p.Pro1182Ala
XM_005245812.1:c.3532C>G	XP_005245869.1:p.Pro1178Ala
XM_005245813.1:c.3499C>G	XP_005245870.1:p.Pro1167Ala
XM_005245815.1:c.3442C>G	XP_005245872.1:p.Pro1148Ala
XM_006710512.1:c.3541C>G	XP_006710575.1:p.Pro1181Ala
XM_006710513.1:c.3517C>G	XP_006710576.1:p.Pro1173Ala
XM_011541128.1:c.3544C>G	XP_011539430.1:p.Pro1182Ala
XM_011541129.1:c.3352C>G	XP_011539431.1:p.Pro1118Ala
XM_017000844.1:c.*186C>G	XP_016856333.1:n.*186C>G
XM_017000845.1:c.*186C>G	XP_016856334.1:n.*186C>G
XM_017000846.1:c.*186C>G	XP_016856335.1:n.*186C>G
XM_017000847.1:c.*186C>G	XP_016856336.1:n.*186C>G
XM_017000848.1:c.*186C>G	XP_016856337.1:n.*186C>G
XM_017000849.1:c.*186C>G	XP_016856338.1:n.*186C>G
XM_017000850.1:c.*186C>G	XP_016856339.1:n.*186C>G
NM_022089.4:c.*186C>G MANE Select	NP_071372.1:n.*186C>G
NM_001141973.3:c.*186C>G	NP_001135445.1:n.*186C>G
NM_001141974.3:c.3427C>G	NP_001135446.1:p.Pro1143Ala