Canonical Allele Identifier: CA338233555

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17313369A>C (hg19) ; chr1:g.16986874A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986874A>C , CM000663.2:g.16986874A>C	GRCh38
NC_000001.10:g.17313369A>C , CM000663.1:g.17313369A>C	GRCh37
NC_000001.9:g.17185956A>C	NCBI36
NG_009054.1:g.30055T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3166T>G MANE Select	ENSP00000327214.8:p.Phe1056Val
ENST00000326735.12:c.3166T>G	ENSP00000327214.8:p.Phe1056Val
ENST00000341676.9:c.3034T>G	ENSP00000341115.5:p.Phe1012Val
ENST00000452699.5:c.3151T>G	ENSP00000413307.1:p.Phe1051Val
ENST00000466561.1:n.1040T>G
ENST00000502418.1:c.754T>G	ENSP00000423065.1:p.Phe252Val
NM_001141973.2:c.3151T>G	NP_001135445.1:p.Phe1051Val
NM_001141974.2:c.3034T>G	NP_001135446.1:p.Phe1012Val
NM_022089.3:c.3166T>G	NP_071372.1:p.Phe1056Val
XM_005245809.1:c.3166T>G	XP_005245866.1:p.Phe1056Val
XM_005245810.1:c.3163T>G	XP_005245867.1:p.Phe1055Val
XM_005245811.1:c.3151T>G	XP_005245868.1:p.Phe1051Val
XM_005245812.1:c.3139T>G	XP_005245869.1:p.Phe1047Val
XM_005245813.1:c.3106T>G	XP_005245870.1:p.Phe1036Val
XM_005245815.1:c.3049T>G	XP_005245872.1:p.Phe1017Val
XM_006710512.1:c.3148T>G	XP_006710575.1:p.Phe1050Val
XM_006710513.1:c.3124T>G	XP_006710576.1:p.Phe1042Val
XM_011541128.1:c.3151T>G	XP_011539430.1:p.Phe1051Val
XM_011541129.1:c.2959T>G	XP_011539431.1:p.Phe987Val
XM_017000844.1:c.3151T>G	XP_016856333.1:p.Phe1051Val
XM_017000845.1:c.3148T>G	XP_016856334.1:p.Phe1050Val
XM_017000846.1:c.3124T>G	XP_016856335.1:p.Phe1042Val
XM_017000847.1:c.3121T>G	XP_016856336.1:p.Phe1041Val
XM_017000848.1:c.3049T>G	XP_016856337.1:p.Phe1017Val
XM_017000849.1:c.3034T>G	XP_016856338.1:p.Phe1012Val
XM_017000850.1:c.2959T>G	XP_016856339.1:p.Phe987Val
NM_022089.4:c.3166T>G MANE Select	NP_071372.1:p.Phe1056Val
NM_001141973.3:c.3151T>G	NP_001135445.1:p.Phe1051Val
NM_001141974.3:c.3034T>G	NP_001135446.1:p.Phe1012Val