Canonical Allele Identifier: CA355784040

Gene: ATP13A4

Linked Data

• MyVariant Identifiers: chr3:g.193185245A>G (hg19) ; chr3:g.193467456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467456A>G , CM000665.2:g.193467456A>G	GRCh38
NC_000003.11:g.193185245A>G , CM000665.1:g.193185245A>G	GRCh37
NC_000003.10:g.194667939A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.974T>C MANE Select	ENSP00000339182.4:p.Leu325Ser
ENST00000295548.3:c.974T>C	ENSP00000295548.3:p.Leu325Ser
ENST00000342695.8:c.974T>C	ENSP00000339182.4:p.Leu325Ser
ENST00000392443.7:c.974T>C	ENSP00000376238.3:p.Leu325Ser
ENST00000450950.6:c.*417T>C	ENSP00000402023.2:n.*417T>C
ENST00000490925.5:n.1082T>C
NM_032279.3:c.974T>C	NP_115655.2:p.Leu325Ser
XM_005247829.2:c.974T>C	XP_005247886.1:p.Leu325Ser
XM_011513232.1:c.974T>C	XP_011511534.1:p.Leu325Ser
XR_241512.2:n.1275T>C
XR_924191.1:n.1275T>C
XM_011513232.2:c.974T>C	XP_011511534.1:p.Leu325Ser
XM_017007318.1:c.647T>C	XP_016862807.1:p.Leu216Ser
XM_017007319.1:c.974T>C	XP_016862808.1:p.Leu325Ser
XR_001740324.2:n.1044T>C
XR_001740325.1:n.1044T>C
XR_002959602.1:n.1208T>C
XR_924191.3:n.1044T>C
NM_032279.4:c.974T>C MANE Select	NP_115655.2:p.Leu325Ser