Canonical Allele Identifier: CA416094109

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17316263G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989768G>C , CM000663.2:g.16989768G>C	GRCh38
NC_000001.10:g.17316263G>C , CM000663.1:g.17316263G>C	GRCh37
NC_000001.9:g.17188850G>C	NCBI36
NG_009054.1:g.27161C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.2532C>G MANE Select	ENSP00000327214.8:p.Val844=
ENST00000326735.12:c.2532C>G	ENSP00000327214.8:p.Val844=
ENST00000341676.9:c.2400C>G	ENSP00000341115.5:p.Val800=
ENST00000452699.5:c.2517C>G	ENSP00000413307.1:p.Val839=
ENST00000466561.1:n.406C>G
ENST00000502418.1:c.120C>G	ENSP00000423065.1:p.Val40=
NM_001141973.2:c.2517C>G	NP_001135445.1:p.Val839=
NM_001141974.2:c.2400C>G	NP_001135446.1:p.Val800=
NM_022089.3:c.2532C>G	NP_071372.1:p.Val844=
XM_005245809.1:c.2532C>G	XP_005245866.1:p.Val844=
XM_005245810.1:c.2529C>G	XP_005245867.1:p.Val843=
XM_005245811.1:c.2517C>G	XP_005245868.1:p.Val839=
XM_005245812.1:c.2505C>G	XP_005245869.1:p.Val835=
XM_005245813.1:c.2472C>G	XP_005245870.1:p.Val824=
XM_005245815.1:c.2415C>G	XP_005245872.1:p.Val805=
XM_006710512.1:c.2514C>G	XP_006710575.1:p.Val838=
XM_006710513.1:c.2490C>G	XP_006710576.1:p.Val830=
XM_011541128.1:c.2517C>G	XP_011539430.1:p.Val839=
XM_011541129.1:c.2325C>G	XP_011539431.1:p.Val775=
XM_017000844.1:c.2517C>G	XP_016856333.1:p.Val839=
XM_017000845.1:c.2514C>G	XP_016856334.1:p.Val838=
XM_017000846.1:c.2490C>G	XP_016856335.1:p.Val830=
XM_017000847.1:c.2487C>G	XP_016856336.1:p.Val829=
XM_017000848.1:c.2415C>G	XP_016856337.1:p.Val805=
XM_017000849.1:c.2400C>G	XP_016856338.1:p.Val800=
XM_017000850.1:c.2325C>G	XP_016856339.1:p.Val775=
NM_022089.4:c.2532C>G MANE Select	NP_071372.1:p.Val844=
NM_001141973.3:c.2517C>G	NP_001135445.1:p.Val839=
NM_001141974.3:c.2400C>G	NP_001135446.1:p.Val800=