Canonical Allele Identifier: CA1156021161

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989788_16989791delinsTGGG , CM000663.2:g.16989788_16989791delinsTGGG	GRCh38
NC_000001.10:g.17316283_17316286delinsTGGG , CM000663.1:g.17316283_17316286delinsTGGG	GRCh37
NC_000001.9:g.17188870_17188873delinsTGGG	NCBI36
NG_009054.1:g.27138_27141delinsCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.2530-21_2530-18delinsCCCA MANE Select	ENSP00000327214.8:n.2530-21_2530-18delinsCCCA
ENST00000326735.12:c.2530-21_2530-18delinsCCCA	ENSP00000327214.8:n.2530-21_2530-18delinsCCCA
ENST00000341676.9:c.2398-21_2398-18delinsCCCA	ENSP00000341115.5:n.2398-21_2398-18delinsCCCA
ENST00000452699.5:c.2515-21_2515-18delinsCCCA	ENSP00000413307.1:n.2515-21_2515-18delinsCCCA
ENST00000466561.1:n.404-21_404-18delinsCCCA
ENST00000502418.1:c.118-21_118-18delinsCCCA	ENSP00000423065.1:n.118-21_118-18delinsCCCA
NM_001141973.2:c.2515-21_2515-18delinsCCCA	NP_001135445.1:n.2515-21_2515-18delinsCCCA
NM_001141974.2:c.2398-21_2398-18delinsCCCA	NP_001135446.1:n.2398-21_2398-18delinsCCCA
NM_022089.3:c.2530-21_2530-18delinsCCCA	NP_071372.1:n.2530-21_2530-18delinsCCCA
XM_005245809.1:c.2530-21_2530-18delinsCCCA	XP_005245866.1:n.2530-21_2530-18delinsCCCA
XM_005245810.1:c.2527-21_2527-18delinsCCCA	XP_005245867.1:n.2527-21_2527-18delinsCCCA
XM_005245811.1:c.2515-21_2515-18delinsCCCA	XP_005245868.1:n.2515-21_2515-18delinsCCCA
XM_005245812.1:c.2503-21_2503-18delinsCCCA	XP_005245869.1:n.2503-21_2503-18delinsCCCA
XM_005245813.1:c.2470-21_2470-18delinsCCCA	XP_005245870.1:n.2470-21_2470-18delinsCCCA
XM_005245815.1:c.2413-21_2413-18delinsCCCA	XP_005245872.1:n.2413-21_2413-18delinsCCCA
XM_006710512.1:c.2512-21_2512-18delinsCCCA	XP_006710575.1:n.2512-21_2512-18delinsCCCA
XM_006710513.1:c.2488-21_2488-18delinsCCCA	XP_006710576.1:n.2488-21_2488-18delinsCCCA
XM_011541128.1:c.2515-21_2515-18delinsCCCA	XP_011539430.1:n.2515-21_2515-18delinsCCCA
XM_011541129.1:c.2323-21_2323-18delinsCCCA	XP_011539431.1:n.2323-21_2323-18delinsCCCA
XM_017000844.1:c.2515-21_2515-18delinsCCCA	XP_016856333.1:n.2515-21_2515-18delinsCCCA
XM_017000845.1:c.2512-21_2512-18delinsCCCA	XP_016856334.1:n.2512-21_2512-18delinsCCCA
XM_017000846.1:c.2488-21_2488-18delinsCCCA	XP_016856335.1:n.2488-21_2488-18delinsCCCA
XM_017000847.1:c.2485-21_2485-18delinsCCCA	XP_016856336.1:n.2485-21_2485-18delinsCCCA
XM_017000848.1:c.2413-21_2413-18delinsCCCA	XP_016856337.1:n.2413-21_2413-18delinsCCCA
XM_017000849.1:c.2398-21_2398-18delinsCCCA	XP_016856338.1:n.2398-21_2398-18delinsCCCA
XM_017000850.1:c.2323-21_2323-18delinsCCCA	XP_016856339.1:n.2323-21_2323-18delinsCCCA
NM_022089.4:c.2530-21_2530-18delinsCCCA MANE Select	NP_071372.1:n.2530-21_2530-18delinsCCCA
NM_001141973.3:c.2515-21_2515-18delinsCCCA	NP_001135445.1:n.2515-21_2515-18delinsCCCA
NM_001141974.3:c.2398-21_2398-18delinsCCCA	NP_001135446.1:n.2398-21_2398-18delinsCCCA