Canonical Allele Identifier: CA2758546
Gene: ATP13A4 HGNC NCBI

Linked Data

dbSNP Id: rs375205989

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.193467442T>C , CM000665.2:g.193467442T>C GRCh38
NC_000003.11:g.193185231T>C , CM000665.1:g.193185231T>C GRCh37
NC_000003.10:g.194667925T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342695.9:c.988A>G MANE Select ENSP00000339182.4:p.Ser330Gly
ENST00000295548.3:c.988A>G ENSP00000295548.3:p.Ser330Gly
ENST00000342695.8:c.988A>G ENSP00000339182.4:p.Ser330Gly
ENST00000392443.7:c.988A>G ENSP00000376238.3:p.Ser330Gly
ENST00000450950.6:c.*431A>G ENSP00000402023.2:n.*431A>G
ENST00000490925.5:n.1096A>G
NM_032279.3:c.988A>G NP_115655.2:p.Ser330Gly
XM_005247829.2:c.988A>G XP_005247886.1:p.Ser330Gly
XM_011513232.1:c.988A>G XP_011511534.1:p.Ser330Gly
XR_241512.2:n.1289A>G
XR_924191.1:n.1289A>G
XM_011513232.2:c.988A>G XP_011511534.1:p.Ser330Gly
XM_017007318.1:c.661A>G XP_016862807.1:p.Ser221Gly
XM_017007319.1:c.988A>G XP_016862808.1:p.Ser330Gly
XR_001740324.2:n.1058A>G
XR_001740325.1:n.1058A>G
XR_002959602.1:n.1222A>G
XR_924191.3:n.1058A>G
NM_032279.4:c.988A>G MANE Select NP_115655.2:p.Ser330Gly