Canonical Allele Identifier: CA636437

Gene: ATP13A2

Linked Data

• dbSNP Id: rs766726551
• ExAC: 1:17312655 G / A
• gnomAD v2: 1-17312655-G-A
• gnomAD v3: 1-16986160-G-A
• gnomAD v4: 1-16986160-G-A
• MyVariant Identifiers: chr1:g.17312655G>A (hg19) ; chr1:g.16986160G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986160G>A , CM000663.2:g.16986160G>A	GRCh38
NC_000001.10:g.17312655G>A , CM000663.1:g.17312655G>A	GRCh37
NC_000001.9:g.17185242G>A	NCBI36
NG_009054.1:g.30769C>T
NG_029688.1:g.427C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.*61C>T MANE Select	ENSP00000327214.8:n.*61C>T
ENST00000326735.12:c.*61C>T	ENSP00000327214.8:n.*61C>T
ENST00000341676.9:c.3302C>T	ENSP00000341115.5:p.Pro1101Leu
ENST00000452699.5:c.*61C>T	ENSP00000413307.1:n.*61C>T
ENST00000466561.1:n.1650C>T
ENST00000502418.1:c.1022C>T	ENSP00000423065.1:p.Pro341Leu
NM_001141973.2:c.*61C>T	NP_001135445.1:n.*61C>T
NM_001141974.2:c.3302C>T	NP_001135446.1:p.Pro1101Leu
NM_022089.3:c.*61C>T	NP_071372.1:n.*61C>T
XM_005245809.1:c.3434C>T	XP_005245866.1:p.Pro1145Leu
XM_005245810.1:c.3431C>T	XP_005245867.1:p.Pro1144Leu
XM_005245811.1:c.3419C>T	XP_005245868.1:p.Pro1140Leu
XM_005245812.1:c.3407C>T	XP_005245869.1:p.Pro1136Leu
XM_005245813.1:c.3374C>T	XP_005245870.1:p.Pro1125Leu
XM_005245815.1:c.3317C>T	XP_005245872.1:p.Pro1106Leu
XM_006710512.1:c.3416C>T	XP_006710575.1:p.Pro1139Leu
XM_006710513.1:c.3392C>T	XP_006710576.1:p.Pro1131Leu
XM_011541128.1:c.3419C>T	XP_011539430.1:p.Pro1140Leu
XM_011541129.1:c.3227C>T	XP_011539431.1:p.Pro1076Leu
XM_017000844.1:c.*61C>T	XP_016856333.1:n.*61C>T
XM_017000845.1:c.*61C>T	XP_016856334.1:n.*61C>T
XM_017000846.1:c.*61C>T	XP_016856335.1:n.*61C>T
XM_017000847.1:c.*61C>T	XP_016856336.1:n.*61C>T
XM_017000848.1:c.*61C>T	XP_016856337.1:n.*61C>T
XM_017000849.1:c.*61C>T	XP_016856338.1:n.*61C>T
XM_017000850.1:c.*61C>T	XP_016856339.1:n.*61C>T
NM_022089.4:c.*61C>T MANE Select	NP_071372.1:n.*61C>T
NM_001141973.3:c.*61C>T	NP_001135445.1:n.*61C>T
NM_001141974.3:c.3302C>T	NP_001135446.1:p.Pro1101Leu