Canonical Allele Identifier: CA1156050599

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986924_16986926delinsGGT , CM000663.2:g.16986924_16986926delinsGGT	GRCh38
NC_000001.10:g.17313419_17313421delinsGGT , CM000663.1:g.17313419_17313421delinsGGT	GRCh37
NC_000001.9:g.17186006_17186008delinsGGT	NCBI36
NG_009054.1:g.30003_30005delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3114_3116delinsACC MANE Select	ENSP00000327214.8:p.Ala1038=
ENST00000326735.12:c.3114_3116delinsACC	ENSP00000327214.8:p.Ala1038=
ENST00000341676.9:c.2982_2984delinsACC	ENSP00000341115.5:p.Ala994=
ENST00000452699.5:c.3099_3101delinsACC	ENSP00000413307.1:p.Ala1033=
ENST00000466561.1:n.988_990delinsACC
ENST00000502418.1:c.702_704delinsACC	ENSP00000423065.1:p.Ala234=
NM_001141973.2:c.3099_3101delinsACC	NP_001135445.1:p.Ala1033=
NM_001141974.2:c.2982_2984delinsACC	NP_001135446.1:p.Ala994=
NM_022089.3:c.3114_3116delinsACC	NP_071372.1:p.Ala1038=
XM_005245809.1:c.3114_3116delinsACC	XP_005245866.1:p.Ala1038=
XM_005245810.1:c.3111_3113delinsACC	XP_005245867.1:p.Ala1037=
XM_005245811.1:c.3099_3101delinsACC	XP_005245868.1:p.Ala1033=
XM_005245812.1:c.3087_3089delinsACC	XP_005245869.1:p.Ala1029=
XM_005245813.1:c.3054_3056delinsACC	XP_005245870.1:p.Ala1018=
XM_005245815.1:c.2997_2999delinsACC	XP_005245872.1:p.Ala999=
XM_006710512.1:c.3096_3098delinsACC	XP_006710575.1:p.Ala1032=
XM_006710513.1:c.3072_3074delinsACC	XP_006710576.1:p.Ala1024=
XM_011541128.1:c.3099_3101delinsACC	XP_011539430.1:p.Ala1033=
XM_011541129.1:c.2907_2909delinsACC	XP_011539431.1:p.Ala969=
XM_017000844.1:c.3099_3101delinsACC	XP_016856333.1:p.Ala1033=
XM_017000845.1:c.3096_3098delinsACC	XP_016856334.1:p.Ala1032=
XM_017000846.1:c.3072_3074delinsACC	XP_016856335.1:p.Ala1024=
XM_017000847.1:c.3069_3071delinsACC	XP_016856336.1:p.Ala1023=
XM_017000848.1:c.2997_2999delinsACC	XP_016856337.1:p.Ala999=
XM_017000849.1:c.2982_2984delinsACC	XP_016856338.1:p.Ala994=
XM_017000850.1:c.2907_2909delinsACC	XP_016856339.1:p.Ala969=
NM_022089.4:c.3114_3116delinsACC MANE Select	NP_071372.1:p.Ala1038=
NM_001141973.3:c.3099_3101delinsACC	NP_001135445.1:p.Ala1033=
NM_001141974.3:c.2982_2984delinsACC	NP_001135446.1:p.Ala994=