Canonical Allele Identifier: CA437431052

Gene: ATP13A4

Linked Data

• MyVariant Identifiers: chr3:g.193185262T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193467473T>G , CM000665.2:g.193467473T>G	GRCh38
NC_000003.11:g.193185262T>G , CM000665.1:g.193185262T>G	GRCh37
NC_000003.10:g.194667956T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342695.9:c.957A>C MANE Select	ENSP00000339182.4:p.Pro319=
ENST00000295548.3:c.957A>C	ENSP00000295548.3:p.Pro319=
ENST00000342695.8:c.957A>C	ENSP00000339182.4:p.Pro319=
ENST00000392443.7:c.957A>C	ENSP00000376238.3:p.Pro319=
ENST00000450950.6:c.*400A>C	ENSP00000402023.2:n.*400A>C
ENST00000490925.5:n.1065A>C
NM_032279.3:c.957A>C	NP_115655.2:p.Pro319=
XM_005247829.2:c.957A>C	XP_005247886.1:p.Pro319=
XM_011513232.1:c.957A>C	XP_011511534.1:p.Pro319=
XR_241512.2:n.1258A>C
XR_924191.1:n.1258A>C
XM_011513232.2:c.957A>C	XP_011511534.1:p.Pro319=
XM_017007318.1:c.630A>C	XP_016862807.1:p.Pro210=
XM_017007319.1:c.957A>C	XP_016862808.1:p.Pro319=
XR_001740324.2:n.1027A>C
XR_001740325.1:n.1027A>C
XR_002959602.1:n.1191A>C
XR_924191.3:n.1027A>C
NM_032279.4:c.957A>C MANE Select	NP_115655.2:p.Pro319=