Canonical Allele Identifier: CA338232355

Gene: ATP13A2

Linked Data

• dbSNP Id: rs776147612
• MyVariant Identifiers: chr1:g.17312793T>G (hg19) ; chr1:g.16986298T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986298T>G , CM000663.2:g.16986298T>G	GRCh38
NC_000001.10:g.17312793T>G , CM000663.1:g.17312793T>G	GRCh37
NC_000001.9:g.17185380T>G	NCBI36
NG_009054.1:g.30631A>C
NG_029688.1:g.289A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3466A>C MANE Select	ENSP00000327214.8:p.Lys1156Gln
ENST00000326735.12:c.3466A>C	ENSP00000327214.8:p.Lys1156Gln
ENST00000341676.9:c.3164A>C	ENSP00000341115.5:p.Gln1055Pro
ENST00000452699.5:c.3451A>C	ENSP00000413307.1:p.Lys1151Gln
ENST00000466561.1:n.1512A>C
ENST00000502418.1:c.884A>C	ENSP00000423065.1:p.Gln295Pro
NM_001141973.2:c.3451A>C	NP_001135445.1:p.Lys1151Gln
NM_001141974.2:c.3164A>C	NP_001135446.1:p.Gln1055Pro
NM_022089.3:c.3466A>C	NP_071372.1:p.Lys1156Gln
XM_005245809.1:c.3296A>C	XP_005245866.1:p.Gln1099Pro
XM_005245810.1:c.3293A>C	XP_005245867.1:p.Gln1098Pro
XM_005245811.1:c.3281A>C	XP_005245868.1:p.Gln1094Pro
XM_005245812.1:c.3269A>C	XP_005245869.1:p.Gln1090Pro
XM_005245813.1:c.3236A>C	XP_005245870.1:p.Gln1079Pro
XM_005245815.1:c.3179A>C	XP_005245872.1:p.Gln1060Pro
XM_006710512.1:c.3278A>C	XP_006710575.1:p.Gln1093Pro
XM_006710513.1:c.3254A>C	XP_006710576.1:p.Gln1085Pro
XM_011541128.1:c.3281A>C	XP_011539430.1:p.Gln1094Pro
XM_011541129.1:c.3089A>C	XP_011539431.1:p.Gln1030Pro
XM_017000844.1:c.3451A>C	XP_016856333.1:p.Lys1151Gln
XM_017000845.1:c.3448A>C	XP_016856334.1:p.Lys1150Gln
XM_017000846.1:c.3424A>C	XP_016856335.1:p.Lys1142Gln
XM_017000847.1:c.3421A>C	XP_016856336.1:p.Lys1141Gln
XM_017000848.1:c.3349A>C	XP_016856337.1:p.Lys1117Gln
XM_017000849.1:c.3334A>C	XP_016856338.1:p.Lys1112Gln
XM_017000850.1:c.3259A>C	XP_016856339.1:p.Lys1087Gln
NM_022089.4:c.3466A>C MANE Select	NP_071372.1:p.Lys1156Gln
NM_001141973.3:c.3451A>C	NP_001135445.1:p.Lys1151Gln
NM_001141974.3:c.3164A>C	NP_001135446.1:p.Gln1055Pro