Canonical Allele Identifier: CA338232674

Gene: ATP13A2

Linked Data

• gnomAD v4: 1-16986468-G-T
• MyVariant Identifiers: chr1:g.17312963G>T (hg19) ; chr1:g.16986468G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986468G>T , CM000663.2:g.16986468G>T	GRCh38
NC_000001.10:g.17312963G>T , CM000663.1:g.17312963G>T	GRCh37
NC_000001.9:g.17185550G>T	NCBI36
NG_009054.1:g.30461C>A
NG_029688.1:g.119C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3400C>A MANE Select	ENSP00000327214.8:p.Leu1134Met
ENST00000326735.12:c.3400C>A	ENSP00000327214.8:p.Leu1134Met
ENST00000341676.9:c.3104-110C>A	ENSP00000341115.5:n.3104-110C>A
ENST00000452699.5:c.3385C>A	ENSP00000413307.1:p.Leu1129Met
ENST00000466561.1:n.1446C>A
ENST00000502418.1:c.824-110C>A	ENSP00000423065.1:n.824-110C>A
NM_001141973.2:c.3385C>A	NP_001135445.1:p.Leu1129Met
NM_001141974.2:c.3104-110C>A	NP_001135446.1:n.3104-110C>A
NM_022089.3:c.3400C>A	NP_071372.1:p.Leu1134Met
XM_005245809.1:c.3236-110C>A	XP_005245866.1:n.3236-110C>A
XM_005245810.1:c.3233-110C>A	XP_005245867.1:n.3233-110C>A
XM_005245811.1:c.3221-110C>A	XP_005245868.1:n.3221-110C>A
XM_005245812.1:c.3209-110C>A	XP_005245869.1:n.3209-110C>A
XM_005245813.1:c.3176-110C>A	XP_005245870.1:n.3176-110C>A
XM_005245815.1:c.3119-110C>A	XP_005245872.1:n.3119-110C>A
XM_006710512.1:c.3218-110C>A	XP_006710575.1:n.3218-110C>A
XM_006710513.1:c.3194-110C>A	XP_006710576.1:n.3194-110C>A
XM_011541128.1:c.3221-110C>A	XP_011539430.1:n.3221-110C>A
XM_011541129.1:c.3029-110C>A	XP_011539431.1:n.3029-110C>A
XM_017000844.1:c.3385C>A	XP_016856333.1:p.Leu1129Met
XM_017000845.1:c.3382C>A	XP_016856334.1:p.Leu1128Met
XM_017000846.1:c.3358C>A	XP_016856335.1:p.Leu1120Met
XM_017000847.1:c.3355C>A	XP_016856336.1:p.Leu1119Met
XM_017000848.1:c.3283C>A	XP_016856337.1:p.Leu1095Met
XM_017000849.1:c.3268C>A	XP_016856338.1:p.Leu1090Met
XM_017000850.1:c.3193C>A	XP_016856339.1:p.Leu1065Met
NM_022089.4:c.3400C>A MANE Select	NP_071372.1:p.Leu1134Met
NM_001141973.3:c.3385C>A	NP_001135445.1:p.Leu1129Met
NM_001141974.3:c.3104-110C>A	NP_001135446.1:n.3104-110C>A