Canonical Allele Identifier: CA637026

Gene: ATP13A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16992291C>T , CM000663.2:g.16992291C>T	GRCh38
NC_000001.10:g.17318786C>T , CM000663.1:g.17318786C>T	GRCh37
NC_000001.9:g.17191373C>T	NCBI36
NG_009054.1:g.24638G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1957G>A MANE Select	ENSP00000327214.8:p.Val653Ile
ENST00000326735.12:c.1957G>A	ENSP00000327214.8:p.Val653Ile
ENST00000341676.9:c.1942G>A	ENSP00000341115.5:p.Val648Ile
ENST00000452699.5:c.1942G>A	ENSP00000413307.1:p.Val648Ile
ENST00000503552.1:c.367G>A	ENSP00000421126.1:p.Val123Ile
NM_001141973.2:c.1942G>A	NP_001135445.1:p.Val648Ile
NM_001141974.2:c.1942G>A	NP_001135446.1:p.Val648Ile
NM_022089.3:c.1957G>A	NP_071372.1:p.Val653Ile
XM_005245809.1:c.1957G>A	XP_005245866.1:p.Val653Ile
XM_005245810.1:c.1954G>A	XP_005245867.1:p.Val652Ile
XM_005245811.1:c.1942G>A	XP_005245868.1:p.Val648Ile
XM_005245812.1:c.1930G>A	XP_005245869.1:p.Val644Ile
XM_005245813.1:c.1897G>A	XP_005245870.1:p.Val633Ile
XM_005245815.1:c.1957G>A	XP_005245872.1:p.Val653Ile
XM_006710512.1:c.1939G>A	XP_006710575.1:p.Val647Ile
XM_006710513.1:c.1915G>A	XP_006710576.1:p.Val639Ile
XM_011541128.1:c.1942G>A	XP_011539430.1:p.Val648Ile
XM_011541129.1:c.1750G>A	XP_011539431.1:p.Val584Ile
XM_017000844.1:c.1942G>A	XP_016856333.1:p.Val648Ile
XM_017000845.1:c.1939G>A	XP_016856334.1:p.Val647Ile
XM_017000846.1:c.1915G>A	XP_016856335.1:p.Val639Ile
XM_017000847.1:c.1912G>A	XP_016856336.1:p.Val638Ile
XM_017000848.1:c.1957G>A	XP_016856337.1:p.Val653Ile
XM_017000849.1:c.1942G>A	XP_016856338.1:p.Val648Ile
XM_017000850.1:c.1750G>A	XP_016856339.1:p.Val584Ile
NM_022089.4:c.1957G>A MANE Select	NP_071372.1:p.Val653Ile
NM_001141973.3:c.1942G>A	NP_001135445.1:p.Val648Ile
NM_001141974.3:c.1942G>A	NP_001135446.1:p.Val648Ile