Canonical Allele Identifier: CA1156050701

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986972_16986973delinsTG , CM000663.2:g.16986972_16986973delinsTG	GRCh38
NC_000001.10:g.17313467_17313468delinsTG , CM000663.1:g.17313467_17313468delinsTG	GRCh37
NC_000001.9:g.17186054_17186055delinsTG	NCBI36
NG_009054.1:g.29956_29957delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3084-17_3084-16delinsCA MANE Select	ENSP00000327214.8:n.3084-17_3084-16delinsCA
ENST00000326735.12:c.3084-17_3084-16delinsCA	ENSP00000327214.8:n.3084-17_3084-16delinsCA
ENST00000341676.9:c.2952-17_2952-16delinsCA	ENSP00000341115.5:n.2952-17_2952-16delinsCA
ENST00000452699.5:c.3069-17_3069-16delinsCA	ENSP00000413307.1:n.3069-17_3069-16delinsCA
ENST00000466561.1:n.958-17_958-16delinsCA
ENST00000502418.1:c.672-17_672-16delinsCA	ENSP00000423065.1:n.672-17_672-16delinsCA
NM_001141973.2:c.3069-17_3069-16delinsCA	NP_001135445.1:n.3069-17_3069-16delinsCA
NM_001141974.2:c.2952-17_2952-16delinsCA	NP_001135446.1:n.2952-17_2952-16delinsCA
NM_022089.3:c.3084-17_3084-16delinsCA	NP_071372.1:n.3084-17_3084-16delinsCA
XM_005245809.1:c.3084-17_3084-16delinsCA	XP_005245866.1:n.3084-17_3084-16delinsCA
XM_005245810.1:c.3081-17_3081-16delinsCA	XP_005245867.1:n.3081-17_3081-16delinsCA
XM_005245811.1:c.3069-17_3069-16delinsCA	XP_005245868.1:n.3069-17_3069-16delinsCA
XM_005245812.1:c.3057-17_3057-16delinsCA	XP_005245869.1:n.3057-17_3057-16delinsCA
XM_005245813.1:c.3024-17_3024-16delinsCA	XP_005245870.1:n.3024-17_3024-16delinsCA
XM_005245815.1:c.2967-17_2967-16delinsCA	XP_005245872.1:n.2967-17_2967-16delinsCA
XM_006710512.1:c.3066-17_3066-16delinsCA	XP_006710575.1:n.3066-17_3066-16delinsCA
XM_006710513.1:c.3042-17_3042-16delinsCA	XP_006710576.1:n.3042-17_3042-16delinsCA
XM_011541128.1:c.3069-17_3069-16delinsCA	XP_011539430.1:n.3069-17_3069-16delinsCA
XM_011541129.1:c.2877-17_2877-16delinsCA	XP_011539431.1:n.2877-17_2877-16delinsCA
XM_017000844.1:c.3069-17_3069-16delinsCA	XP_016856333.1:n.3069-17_3069-16delinsCA
XM_017000845.1:c.3066-17_3066-16delinsCA	XP_016856334.1:n.3066-17_3066-16delinsCA
XM_017000846.1:c.3042-17_3042-16delinsCA	XP_016856335.1:n.3042-17_3042-16delinsCA
XM_017000847.1:c.3039-17_3039-16delinsCA	XP_016856336.1:n.3039-17_3039-16delinsCA
XM_017000848.1:c.2967-17_2967-16delinsCA	XP_016856337.1:n.2967-17_2967-16delinsCA
XM_017000849.1:c.2952-17_2952-16delinsCA	XP_016856338.1:n.2952-17_2952-16delinsCA
XM_017000850.1:c.2877-17_2877-16delinsCA	XP_016856339.1:n.2877-17_2877-16delinsCA
NM_022089.4:c.3084-17_3084-16delinsCA MANE Select	NP_071372.1:n.3084-17_3084-16delinsCA
NM_001141973.3:c.3069-17_3069-16delinsCA	NP_001135445.1:n.3069-17_3069-16delinsCA
NM_001141974.3:c.2952-17_2952-16delinsCA	NP_001135446.1:n.2952-17_2952-16delinsCA