Canonical Allele Identifier: CA338239751

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17316246A>G (hg19) ; chr1:g.16989751A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989751A>G , CM000663.2:g.16989751A>G	GRCh38
NC_000001.10:g.17316246A>G , CM000663.1:g.17316246A>G	GRCh37
NC_000001.9:g.17188833A>G	NCBI36
NG_009054.1:g.27178T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.2549T>C MANE Select	ENSP00000327214.8:p.Val850Ala
ENST00000326735.12:c.2549T>C	ENSP00000327214.8:p.Val850Ala
ENST00000341676.9:c.2417T>C	ENSP00000341115.5:p.Val806Ala
ENST00000452699.5:c.2534T>C	ENSP00000413307.1:p.Val845Ala
ENST00000466561.1:n.423T>C
ENST00000502418.1:c.137T>C	ENSP00000423065.1:p.Val46Ala
NM_001141973.2:c.2534T>C	NP_001135445.1:p.Val845Ala
NM_001141974.2:c.2417T>C	NP_001135446.1:p.Val806Ala
NM_022089.3:c.2549T>C	NP_071372.1:p.Val850Ala
XM_005245809.1:c.2549T>C	XP_005245866.1:p.Val850Ala
XM_005245810.1:c.2546T>C	XP_005245867.1:p.Val849Ala
XM_005245811.1:c.2534T>C	XP_005245868.1:p.Val845Ala
XM_005245812.1:c.2522T>C	XP_005245869.1:p.Val841Ala
XM_005245813.1:c.2489T>C	XP_005245870.1:p.Val830Ala
XM_005245815.1:c.2432T>C	XP_005245872.1:p.Val811Ala
XM_006710512.1:c.2531T>C	XP_006710575.1:p.Val844Ala
XM_006710513.1:c.2507T>C	XP_006710576.1:p.Val836Ala
XM_011541128.1:c.2534T>C	XP_011539430.1:p.Val845Ala
XM_011541129.1:c.2342T>C	XP_011539431.1:p.Val781Ala
XM_017000844.1:c.2534T>C	XP_016856333.1:p.Val845Ala
XM_017000845.1:c.2531T>C	XP_016856334.1:p.Val844Ala
XM_017000846.1:c.2507T>C	XP_016856335.1:p.Val836Ala
XM_017000847.1:c.2504T>C	XP_016856336.1:p.Val835Ala
XM_017000848.1:c.2432T>C	XP_016856337.1:p.Val811Ala
XM_017000849.1:c.2417T>C	XP_016856338.1:p.Val806Ala
XM_017000850.1:c.2342T>C	XP_016856339.1:p.Val781Ala
NM_022089.4:c.2549T>C MANE Select	NP_071372.1:p.Val850Ala
NM_001141973.3:c.2534T>C	NP_001135445.1:p.Val845Ala
NM_001141974.3:c.2417T>C	NP_001135446.1:p.Val806Ala