Canonical Allele Identifier: CA416093582

Gene: ATP13A2

Linked Data

• dbSNP Id: rs1474043780
• gnomAD v2: 1-17312991-G-A
• MyVariant Identifiers: chr1:g.17312991G>A (hg19) ; chr1:g.16986496G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986496G>A , CM000663.2:g.16986496G>A	GRCh38
NC_000001.10:g.17312991G>A , CM000663.1:g.17312991G>A	GRCh37
NC_000001.9:g.17185578G>A	NCBI36
NG_009054.1:g.30433C>T
NG_029688.1:g.91C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3372C>T MANE Select	ENSP00000327214.8:p.Val1124=
ENST00000326735.12:c.3372C>T	ENSP00000327214.8:p.Val1124=
ENST00000341676.9:c.3104-138C>T	ENSP00000341115.5:n.3104-138C>T
ENST00000452699.5:c.3357C>T	ENSP00000413307.1:p.Val1119=
ENST00000466561.1:n.1418C>T
ENST00000502418.1:c.824-138C>T	ENSP00000423065.1:n.824-138C>T
NM_001141973.2:c.3357C>T	NP_001135445.1:p.Val1119=
NM_001141974.2:c.3104-138C>T	NP_001135446.1:n.3104-138C>T
NM_022089.3:c.3372C>T	NP_071372.1:p.Val1124=
XM_005245809.1:c.3236-138C>T	XP_005245866.1:n.3236-138C>T
XM_005245810.1:c.3233-138C>T	XP_005245867.1:n.3233-138C>T
XM_005245811.1:c.3221-138C>T	XP_005245868.1:n.3221-138C>T
XM_005245812.1:c.3209-138C>T	XP_005245869.1:n.3209-138C>T
XM_005245813.1:c.3176-138C>T	XP_005245870.1:n.3176-138C>T
XM_005245815.1:c.3119-138C>T	XP_005245872.1:n.3119-138C>T
XM_006710512.1:c.3218-138C>T	XP_006710575.1:n.3218-138C>T
XM_006710513.1:c.3194-138C>T	XP_006710576.1:n.3194-138C>T
XM_011541128.1:c.3221-138C>T	XP_011539430.1:n.3221-138C>T
XM_011541129.1:c.3029-138C>T	XP_011539431.1:n.3029-138C>T
XM_017000844.1:c.3357C>T	XP_016856333.1:p.Val1119=
XM_017000845.1:c.3354C>T	XP_016856334.1:p.Val1118=
XM_017000846.1:c.3330C>T	XP_016856335.1:p.Val1110=
XM_017000847.1:c.3327C>T	XP_016856336.1:p.Val1109=
XM_017000848.1:c.3255C>T	XP_016856337.1:p.Val1085=
XM_017000849.1:c.3240C>T	XP_016856338.1:p.Val1080=
XM_017000850.1:c.3165C>T	XP_016856339.1:p.Val1055=
NM_022089.4:c.3372C>T MANE Select	NP_071372.1:p.Val1124=
NM_001141973.3:c.3357C>T	NP_001135445.1:p.Val1119=
NM_001141974.3:c.3104-138C>T	NP_001135446.1:n.3104-138C>T