Canonical Allele Identifier: CA338232487

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312826A>G (hg19) ; chr1:g.16986331A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986331A>G , CM000663.2:g.16986331A>G	GRCh38
NC_000001.10:g.17312826A>G , CM000663.1:g.17312826A>G	GRCh37
NC_000001.9:g.17185413A>G	NCBI36
NG_009054.1:g.30598T>C
NG_029688.1:g.256T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3433T>C MANE Select	ENSP00000327214.8:p.Cys1145Arg
ENST00000326735.12:c.3433T>C	ENSP00000327214.8:p.Cys1145Arg
ENST00000341676.9:c.3131T>C	ENSP00000341115.5:p.Leu1044Pro
ENST00000452699.5:c.3418T>C	ENSP00000413307.1:p.Cys1140Arg
ENST00000466561.1:n.1479T>C
ENST00000502418.1:c.851T>C	ENSP00000423065.1:p.Leu284Pro
NM_001141973.2:c.3418T>C	NP_001135445.1:p.Cys1140Arg
NM_001141974.2:c.3131T>C	NP_001135446.1:p.Leu1044Pro
NM_022089.3:c.3433T>C	NP_071372.1:p.Cys1145Arg
XM_005245809.1:c.3263T>C	XP_005245866.1:p.Leu1088Pro
XM_005245810.1:c.3260T>C	XP_005245867.1:p.Leu1087Pro
XM_005245811.1:c.3248T>C	XP_005245868.1:p.Leu1083Pro
XM_005245812.1:c.3236T>C	XP_005245869.1:p.Leu1079Pro
XM_005245813.1:c.3203T>C	XP_005245870.1:p.Leu1068Pro
XM_005245815.1:c.3146T>C	XP_005245872.1:p.Leu1049Pro
XM_006710512.1:c.3245T>C	XP_006710575.1:p.Leu1082Pro
XM_006710513.1:c.3221T>C	XP_006710576.1:p.Leu1074Pro
XM_011541128.1:c.3248T>C	XP_011539430.1:p.Leu1083Pro
XM_011541129.1:c.3056T>C	XP_011539431.1:p.Leu1019Pro
XM_017000844.1:c.3418T>C	XP_016856333.1:p.Cys1140Arg
XM_017000845.1:c.3415T>C	XP_016856334.1:p.Cys1139Arg
XM_017000846.1:c.3391T>C	XP_016856335.1:p.Cys1131Arg
XM_017000847.1:c.3388T>C	XP_016856336.1:p.Cys1130Arg
XM_017000848.1:c.3316T>C	XP_016856337.1:p.Cys1106Arg
XM_017000849.1:c.3301T>C	XP_016856338.1:p.Cys1101Arg
XM_017000850.1:c.3226T>C	XP_016856339.1:p.Cys1076Arg
NM_022089.4:c.3433T>C MANE Select	NP_071372.1:p.Cys1145Arg
NM_001141973.3:c.3418T>C	NP_001135445.1:p.Cys1140Arg
NM_001141974.3:c.3131T>C	NP_001135446.1:p.Leu1044Pro