Canonical Allele Identifier: CA355784059

Gene: ATP13A4

Linked Data

• MyVariant Identifiers: chr3:g.193185254T>G (hg19) ; chr3:g.193467465T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467465T>G , CM000665.2:g.193467465T>G	GRCh38
NC_000003.11:g.193185254T>G , CM000665.1:g.193185254T>G	GRCh37
NC_000003.10:g.194667948T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.965A>C MANE Select	ENSP00000339182.4:p.Lys322Thr
ENST00000295548.3:c.965A>C	ENSP00000295548.3:p.Lys322Thr
ENST00000342695.8:c.965A>C	ENSP00000339182.4:p.Lys322Thr
ENST00000392443.7:c.965A>C	ENSP00000376238.3:p.Lys322Thr
ENST00000450950.6:c.*408A>C	ENSP00000402023.2:n.*408A>C
ENST00000490925.5:n.1073A>C
NM_032279.3:c.965A>C	NP_115655.2:p.Lys322Thr
XM_005247829.2:c.965A>C	XP_005247886.1:p.Lys322Thr
XM_011513232.1:c.965A>C	XP_011511534.1:p.Lys322Thr
XR_241512.2:n.1266A>C
XR_924191.1:n.1266A>C
XM_011513232.2:c.965A>C	XP_011511534.1:p.Lys322Thr
XM_017007318.1:c.638A>C	XP_016862807.1:p.Lys213Thr
XM_017007319.1:c.965A>C	XP_016862808.1:p.Lys322Thr
XR_001740324.2:n.1035A>C
XR_001740325.1:n.1035A>C
XR_002959602.1:n.1199A>C
XR_924191.3:n.1035A>C
NM_032279.4:c.965A>C MANE Select	NP_115655.2:p.Lys322Thr