Canonical Allele Identifier: CA1144330495

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17004666_17004669delinsGGGG , CM000663.2:g.17004666_17004669delinsGGGG	GRCh38
NC_000001.10:g.17331161_17331164delinsGGGG , CM000663.1:g.17331161_17331164delinsGGGG	GRCh37
NC_000001.9:g.17203748_17203751delinsGGGG	NCBI36
NG_009054.1:g.12260_12263delinsCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.477+23_477+26delinsCCCC MANE Select	ENSP00000327214.8:n.477+23_477+26delinsCCCC
ENST00000326735.12:c.477+23_477+26delinsCCCC	ENSP00000327214.8:n.477+23_477+26delinsCCCC
ENST00000341676.9:c.462+38_462+41delinsCCCC	ENSP00000341115.5:n.462+38_462+41delinsCCCC
ENST00000452699.5:c.462+38_462+41delinsCCCC	ENSP00000413307.1:n.462+38_462+41delinsCCCC
ENST00000508222.5:c.196+38_196+41delinsCCCC
ENST00000509619.1:c.439+38_439+41delinsCCCC
ENST00000510069.5:c.403+23_403+26delinsCCCC
ENST00000511957.5:c.189+23_189+26delinsCCCC	ENSP00000427241.1:n.189+23_189+26delinsCCCC
ENST00000617114.4:c.-385+38_-385+41delinsCCCC	ENSP00000478781.1:n.-385+38_-385+41delinsCCCC
NM_001141973.2:c.462+38_462+41delinsCCCC	NP_001135445.1:n.462+38_462+41delinsCCCC
NM_001141974.2:c.462+38_462+41delinsCCCC	NP_001135446.1:n.462+38_462+41delinsCCCC
NM_022089.3:c.477+23_477+26delinsCCCC	NP_071372.1:n.477+23_477+26delinsCCCC
XM_005245809.1:c.477+23_477+26delinsCCCC	XP_005245866.1:n.477+23_477+26delinsCCCC
XM_005245810.1:c.477+23_477+26delinsCCCC	XP_005245867.1:n.477+23_477+26delinsCCCC
XM_005245811.1:c.462+38_462+41delinsCCCC	XP_005245868.1:n.462+38_462+41delinsCCCC
XM_005245812.1:c.477+23_477+26delinsCCCC	XP_005245869.1:n.477+23_477+26delinsCCCC
XM_005245813.1:c.477+23_477+26delinsCCCC	XP_005245870.1:n.477+23_477+26delinsCCCC
XM_005245815.1:c.477+23_477+26delinsCCCC	XP_005245872.1:n.477+23_477+26delinsCCCC
XM_006710512.1:c.462+38_462+41delinsCCCC	XP_006710575.1:n.462+38_462+41delinsCCCC
XM_006710513.1:c.462+38_462+41delinsCCCC	XP_006710576.1:n.462+38_462+41delinsCCCC
XM_011541128.1:c.477+23_477+26delinsCCCC	XP_011539430.1:n.477+23_477+26delinsCCCC
XM_011541129.1:c.477+23_477+26delinsCCCC	XP_011539431.1:n.477+23_477+26delinsCCCC
XM_017000844.1:c.477+23_477+26delinsCCCC	XP_016856333.1:n.477+23_477+26delinsCCCC
XM_017000845.1:c.462+38_462+41delinsCCCC	XP_016856334.1:n.462+38_462+41delinsCCCC
XM_017000846.1:c.462+38_462+41delinsCCCC	XP_016856335.1:n.462+38_462+41delinsCCCC
XM_017000847.1:c.477+23_477+26delinsCCCC	XP_016856336.1:n.477+23_477+26delinsCCCC
XM_017000848.1:c.477+23_477+26delinsCCCC	XP_016856337.1:n.477+23_477+26delinsCCCC
XM_017000849.1:c.462+38_462+41delinsCCCC	XP_016856338.1:n.462+38_462+41delinsCCCC
XM_017000850.1:c.477+23_477+26delinsCCCC	XP_016856339.1:n.477+23_477+26delinsCCCC
NM_022089.4:c.477+23_477+26delinsCCCC MANE Select	NP_071372.1:n.477+23_477+26delinsCCCC
NM_001141973.3:c.462+38_462+41delinsCCCC	NP_001135445.1:n.462+38_462+41delinsCCCC
NM_001141974.3:c.462+38_462+41delinsCCCC	NP_001135446.1:n.462+38_462+41delinsCCCC