Canonical Allele Identifier: CA338230469

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312524T>A (hg19) ; chr1:g.16986029T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986029T>A , CM000663.2:g.16986029T>A	GRCh38
NC_000001.10:g.17312524T>A , CM000663.1:g.17312524T>A	GRCh37
NC_000001.9:g.17185111T>A	NCBI36
NG_009054.1:g.30900A>T
NG_029688.1:g.558A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.*192A>T MANE Select	ENSP00000327214.8:n.*192A>T
ENST00000326735.12:c.*192A>T	ENSP00000327214.8:n.*192A>T
ENST00000341676.9:c.3433A>T	ENSP00000341115.5:p.Arg1145Trp
ENST00000452699.5:c.*192A>T	ENSP00000413307.1:n.*192A>T
ENST00000466561.1:n.1781A>T
ENST00000502418.1:c.1153A>T	ENSP00000423065.1:p.Arg385Trp
NM_001141973.2:c.*192A>T	NP_001135445.1:n.*192A>T
NM_001141974.2:c.3433A>T	NP_001135446.1:p.Arg1145Trp
NM_022089.3:c.*192A>T	NP_071372.1:n.*192A>T
XM_005245809.1:c.3565A>T	XP_005245866.1:p.Arg1189Trp
XM_005245810.1:c.3562A>T	XP_005245867.1:p.Arg1188Trp
XM_005245811.1:c.3550A>T	XP_005245868.1:p.Arg1184Trp
XM_005245812.1:c.3538A>T	XP_005245869.1:p.Arg1180Trp
XM_005245813.1:c.3505A>T	XP_005245870.1:p.Arg1169Trp
XM_005245815.1:c.3448A>T	XP_005245872.1:p.Arg1150Trp
XM_006710512.1:c.3547A>T	XP_006710575.1:p.Arg1183Trp
XM_006710513.1:c.3523A>T	XP_006710576.1:p.Arg1175Trp
XM_011541128.1:c.3550A>T	XP_011539430.1:p.Arg1184Trp
XM_011541129.1:c.3358A>T	XP_011539431.1:p.Arg1120Trp
XM_017000844.1:c.*192A>T	XP_016856333.1:n.*192A>T
XM_017000845.1:c.*192A>T	XP_016856334.1:n.*192A>T
XM_017000846.1:c.*192A>T	XP_016856335.1:n.*192A>T
XM_017000847.1:c.*192A>T	XP_016856336.1:n.*192A>T
XM_017000848.1:c.*192A>T	XP_016856337.1:n.*192A>T
XM_017000849.1:c.*192A>T	XP_016856338.1:n.*192A>T
XM_017000850.1:c.*192A>T	XP_016856339.1:n.*192A>T
NM_022089.4:c.*192A>T MANE Select	NP_071372.1:n.*192A>T
NM_001141973.3:c.*192A>T	NP_001135445.1:n.*192A>T
NM_001141974.3:c.3433A>T	NP_001135446.1:p.Arg1145Trp