Canonical Allele Identifier: CA416062089

Gene: ATP13A2

Linked Data

• dbSNP Id: rs2077129848
• MyVariant Identifiers: chr1:g.17322978T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16996483T>C , CM000663.2:g.16996483T>C	GRCh38
NC_000001.10:g.17322978T>C , CM000663.1:g.17322978T>C	GRCh37
NC_000001.9:g.17195565T>C	NCBI36
NG_009054.1:g.20446A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1209A>G MANE Select	ENSP00000327214.8:p.Ala403=
ENST00000326735.12:c.1209A>G	ENSP00000327214.8:p.Ala403=
ENST00000341676.9:c.1194A>G	ENSP00000341115.5:p.Ala398=
ENST00000452699.5:c.1194A>G	ENSP00000413307.1:p.Ala398=
ENST00000463860.5:n.817A>G
ENST00000502860.1:n.335-183A>G
ENST00000506174.5:c.356-5A>G	ENSP00000424393.1:n.356-5A>G
ENST00000509392.1:n.212A>G
ENST00000617114.4:c.335-183A>G	ENSP00000478781.1:n.335-183A>G
NM_001141973.2:c.1194A>G	NP_001135445.1:p.Ala398=
NM_001141974.2:c.1194A>G	NP_001135446.1:p.Ala398=
NM_022089.3:c.1209A>G	NP_071372.1:p.Ala403=
XM_005245809.1:c.1209A>G	XP_005245866.1:p.Ala403=
XM_005245810.1:c.1206A>G	XP_005245867.1:p.Ala402=
XM_005245811.1:c.1194A>G	XP_005245868.1:p.Ala398=
XM_005245812.1:c.1182A>G	XP_005245869.1:p.Ala394=
XM_005245813.1:c.1209A>G	XP_005245870.1:p.Ala403=
XM_005245815.1:c.1209A>G	XP_005245872.1:p.Ala403=
XM_006710512.1:c.1191A>G	XP_006710575.1:p.Ala397=
XM_006710513.1:c.1167A>G	XP_006710576.1:p.Ala389=
XM_011541128.1:c.1209A>G	XP_011539430.1:p.Ala403=
XM_011541129.1:c.1209A>G	XP_011539431.1:p.Ala403=
XM_017000844.1:c.1209A>G	XP_016856333.1:p.Ala403=
XM_017000845.1:c.1191A>G	XP_016856334.1:p.Ala397=
XM_017000846.1:c.1167A>G	XP_016856335.1:p.Ala389=
XM_017000847.1:c.1179A>G	XP_016856336.1:p.Ala393=
XM_017000848.1:c.1209A>G	XP_016856337.1:p.Ala403=
XM_017000849.1:c.1194A>G	XP_016856338.1:p.Ala398=
XM_017000850.1:c.1209A>G	XP_016856339.1:p.Ala403=
NM_022089.4:c.1209A>G MANE Select	NP_071372.1:p.Ala403=
NM_001141973.3:c.1194A>G	NP_001135445.1:p.Ala398=
NM_001141974.3:c.1194A>G	NP_001135446.1:p.Ala398=