Canonical Allele Identifier: CA338254959

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17323523G>T (hg19) ; chr1:g.16997028G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16997028G>T , CM000663.2:g.16997028G>T	GRCh38
NC_000001.10:g.17323523G>T , CM000663.1:g.17323523G>T	GRCh37
NC_000001.9:g.17196110G>T	NCBI36
NG_009054.1:g.19901C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.1187C>A MANE Select	ENSP00000327214.8:p.Thr396Asn
ENST00000326735.12:c.1187C>A	ENSP00000327214.8:p.Thr396Asn
ENST00000341676.9:c.1172C>A	ENSP00000341115.5:p.Thr391Asn
ENST00000452699.5:c.1172C>A	ENSP00000413307.1:p.Thr391Asn
ENST00000463860.5:n.795C>A
ENST00000502860.1:n.326C>A
ENST00000506174.5:c.347C>A	ENSP00000424393.1:p.Thr116Asn
ENST00000617114.4:c.326C>A	ENSP00000478781.1:p.Thr109Asn
NM_001141973.2:c.1172C>A	NP_001135445.1:p.Thr391Asn
NM_001141974.2:c.1172C>A	NP_001135446.1:p.Thr391Asn
NM_022089.3:c.1187C>A	NP_071372.1:p.Thr396Asn
XM_005245809.1:c.1187C>A	XP_005245866.1:p.Thr396Asn
XM_005245810.1:c.1184C>A	XP_005245867.1:p.Thr395Asn
XM_005245811.1:c.1172C>A	XP_005245868.1:p.Thr391Asn
XM_005245812.1:c.1160C>A	XP_005245869.1:p.Thr387Asn
XM_005245813.1:c.1187C>A	XP_005245870.1:p.Thr396Asn
XM_005245815.1:c.1187C>A	XP_005245872.1:p.Thr396Asn
XM_006710512.1:c.1169C>A	XP_006710575.1:p.Thr390Asn
XM_006710513.1:c.1145C>A	XP_006710576.1:p.Thr382Asn
XM_011541128.1:c.1187C>A	XP_011539430.1:p.Thr396Asn
XM_011541129.1:c.1187C>A	XP_011539431.1:p.Thr396Asn
XM_017000844.1:c.1187C>A	XP_016856333.1:p.Thr396Asn
XM_017000845.1:c.1169C>A	XP_016856334.1:p.Thr390Asn
XM_017000846.1:c.1145C>A	XP_016856335.1:p.Thr382Asn
XM_017000847.1:c.1157C>A	XP_016856336.1:p.Thr386Asn
XM_017000848.1:c.1187C>A	XP_016856337.1:p.Thr396Asn
XM_017000849.1:c.1172C>A	XP_016856338.1:p.Thr391Asn
XM_017000850.1:c.1187C>A	XP_016856339.1:p.Thr396Asn
NM_022089.4:c.1187C>A MANE Select	NP_071372.1:p.Thr396Asn
NM_001141973.3:c.1172C>A	NP_001135445.1:p.Thr391Asn
NM_001141974.3:c.1172C>A	NP_001135446.1:p.Thr391Asn