Canonical Allele Identifier: CA1430187661

Gene: ATP13A4

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467468G= , CM000665.2:g.193467468G=	GRCh38
NC_000003.11:g.193185257G= , CM000665.1:g.193185257G=	GRCh37
NC_000003.10:g.194667951G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.962C= MANE Select	ENSP00000339182.4:p.Thr321=
ENST00000295548.3:c.962C=	ENSP00000295548.3:p.Thr321=
ENST00000342695.8:c.962C=	ENSP00000339182.4:p.Thr321=
ENST00000392443.7:c.962C=	ENSP00000376238.3:p.Thr321=
ENST00000450950.6:c.*405C=	ENSP00000402023.2:n.*405C=
ENST00000490925.5:n.1070C=
NM_032279.3:c.962C=	NP_115655.2:p.Thr321=
XM_005247829.2:c.962C=	XP_005247886.1:p.Thr321=
XM_011513232.1:c.962C=	XP_011511534.1:p.Thr321=
XR_241512.2:n.1263C=
XR_924191.1:n.1263C=
XM_011513232.2:c.962C=	XP_011511534.1:p.Thr321=
XM_017007318.1:c.635C=	XP_016862807.1:p.Thr212=
XM_017007319.1:c.962C=	XP_016862808.1:p.Thr321=
XR_001740324.2:n.1032C=
XR_001740325.1:n.1032C=
XR_002959602.1:n.1196C=
XR_924191.3:n.1032C=
NM_032279.4:c.962C= MANE Select	NP_115655.2:p.Thr321=