Canonical Allele Identifier: CA338239581

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17316228G>A (hg19) ; chr1:g.16989733G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989733G>A , CM000663.2:g.16989733G>A	GRCh38
NC_000001.10:g.17316228G>A , CM000663.1:g.17316228G>A	GRCh37
NC_000001.9:g.17188815G>A	NCBI36
NG_009054.1:g.27196C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.2567C>T MANE Select	ENSP00000327214.8:p.Pro856Leu
ENST00000326735.12:c.2567C>T	ENSP00000327214.8:p.Pro856Leu
ENST00000341676.9:c.2435C>T	ENSP00000341115.5:p.Pro812Leu
ENST00000452699.5:c.2552C>T	ENSP00000413307.1:p.Pro851Leu
ENST00000466561.1:n.441C>T
ENST00000502418.1:c.155C>T	ENSP00000423065.1:p.Pro52Leu
NM_001141973.2:c.2552C>T	NP_001135445.1:p.Pro851Leu
NM_001141974.2:c.2435C>T	NP_001135446.1:p.Pro812Leu
NM_022089.3:c.2567C>T	NP_071372.1:p.Pro856Leu
XM_005245809.1:c.2567C>T	XP_005245866.1:p.Pro856Leu
XM_005245810.1:c.2564C>T	XP_005245867.1:p.Pro855Leu
XM_005245811.1:c.2552C>T	XP_005245868.1:p.Pro851Leu
XM_005245812.1:c.2540C>T	XP_005245869.1:p.Pro847Leu
XM_005245813.1:c.2507C>T	XP_005245870.1:p.Pro836Leu
XM_005245815.1:c.2450C>T	XP_005245872.1:p.Pro817Leu
XM_006710512.1:c.2549C>T	XP_006710575.1:p.Pro850Leu
XM_006710513.1:c.2525C>T	XP_006710576.1:p.Pro842Leu
XM_011541128.1:c.2552C>T	XP_011539430.1:p.Pro851Leu
XM_011541129.1:c.2360C>T	XP_011539431.1:p.Pro787Leu
XM_017000844.1:c.2552C>T	XP_016856333.1:p.Pro851Leu
XM_017000845.1:c.2549C>T	XP_016856334.1:p.Pro850Leu
XM_017000846.1:c.2525C>T	XP_016856335.1:p.Pro842Leu
XM_017000847.1:c.2522C>T	XP_016856336.1:p.Pro841Leu
XM_017000848.1:c.2450C>T	XP_016856337.1:p.Pro817Leu
XM_017000849.1:c.2435C>T	XP_016856338.1:p.Pro812Leu
XM_017000850.1:c.2360C>T	XP_016856339.1:p.Pro787Leu
NM_022089.4:c.2567C>T MANE Select	NP_071372.1:p.Pro856Leu
NM_001141973.3:c.2552C>T	NP_001135445.1:p.Pro851Leu
NM_001141974.3:c.2435C>T	NP_001135446.1:p.Pro812Leu