Canonical Allele Identifier: CA338233196

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17313110G>C (hg19) ; chr1:g.16986615G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986615G>C , CM000663.2:g.16986615G>C	GRCh38
NC_000001.10:g.17313110G>C , CM000663.1:g.17313110G>C	GRCh37
NC_000001.9:g.17185697G>C	NCBI36
NG_009054.1:g.30314C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3253C>G MANE Select	ENSP00000327214.8:p.Leu1085Val
ENST00000326735.12:c.3253C>G	ENSP00000327214.8:p.Leu1085Val
ENST00000341676.9:c.3103+190C>G	ENSP00000341115.5:n.3103+190C>G
ENST00000452699.5:c.3238C>G	ENSP00000413307.1:p.Leu1080Val
ENST00000466561.1:n.1299C>G
ENST00000502418.1:c.823+190C>G	ENSP00000423065.1:n.823+190C>G
NM_001141973.2:c.3238C>G	NP_001135445.1:p.Leu1080Val
NM_001141974.2:c.3103+190C>G	NP_001135446.1:n.3103+190C>G
NM_022089.3:c.3253C>G	NP_071372.1:p.Leu1085Val
XM_005245809.1:c.3235+190C>G	XP_005245866.1:n.3235+190C>G
XM_005245810.1:c.3232+190C>G	XP_005245867.1:n.3232+190C>G
XM_005245811.1:c.3220+190C>G	XP_005245868.1:n.3220+190C>G
XM_005245812.1:c.3208+190C>G	XP_005245869.1:n.3208+190C>G
XM_005245813.1:c.3175+190C>G	XP_005245870.1:n.3175+190C>G
XM_005245815.1:c.3118+190C>G	XP_005245872.1:n.3118+190C>G
XM_006710512.1:c.3217+190C>G	XP_006710575.1:n.3217+190C>G
XM_006710513.1:c.3193+190C>G	XP_006710576.1:n.3193+190C>G
XM_011541128.1:c.3220+190C>G	XP_011539430.1:n.3220+190C>G
XM_011541129.1:c.3028+190C>G	XP_011539431.1:n.3028+190C>G
XM_017000844.1:c.3238C>G	XP_016856333.1:p.Leu1080Val
XM_017000845.1:c.3235C>G	XP_016856334.1:p.Leu1079Val
XM_017000846.1:c.3211C>G	XP_016856335.1:p.Leu1071Val
XM_017000847.1:c.3208C>G	XP_016856336.1:p.Leu1070Val
XM_017000848.1:c.3136C>G	XP_016856337.1:p.Leu1046Val
XM_017000849.1:c.3121C>G	XP_016856338.1:p.Leu1041Val
XM_017000850.1:c.3046C>G	XP_016856339.1:p.Leu1016Val
NM_022089.4:c.3253C>G MANE Select	NP_071372.1:p.Leu1085Val
NM_001141973.3:c.3238C>G	NP_001135445.1:p.Leu1080Val
NM_001141974.3:c.3103+190C>G	NP_001135446.1:n.3103+190C>G