Canonical Allele Identifier: CA1156049641

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986370_16986371delinsAG , CM000663.2:g.16986370_16986371delinsAG	GRCh38
NC_000001.10:g.17312865_17312866delinsAG , CM000663.1:g.17312865_17312866delinsAG	GRCh37
NC_000001.9:g.17185452_17185453delinsAG	NCBI36
NG_009054.1:g.30558_30559delinsCT
NG_029688.1:g.216_217delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3406-13_3406-12delinsCT MANE Select	ENSP00000327214.8:n.3406-13_3406-12delinsCT
ENST00000326735.12:c.3406-13_3406-12delinsCT	ENSP00000327214.8:n.3406-13_3406-12delinsCT
ENST00000341676.9:c.3104-13_3104-12delinsCT	ENSP00000341115.5:n.3104-13_3104-12delinsCT
ENST00000452699.5:c.3391-13_3391-12delinsCT	ENSP00000413307.1:n.3391-13_3391-12delinsCT
ENST00000466561.1:n.1452-13_1452-12delinsCT
ENST00000502418.1:c.824-13_824-12delinsCT	ENSP00000423065.1:n.824-13_824-12delinsCT
NM_001141973.2:c.3391-13_3391-12delinsCT	NP_001135445.1:n.3391-13_3391-12delinsCT
NM_001141974.2:c.3104-13_3104-12delinsCT	NP_001135446.1:n.3104-13_3104-12delinsCT
NM_022089.3:c.3406-13_3406-12delinsCT	NP_071372.1:n.3406-13_3406-12delinsCT
XM_005245809.1:c.3236-13_3236-12delinsCT	XP_005245866.1:n.3236-13_3236-12delinsCT
XM_005245810.1:c.3233-13_3233-12delinsCT	XP_005245867.1:n.3233-13_3233-12delinsCT
XM_005245811.1:c.3221-13_3221-12delinsCT	XP_005245868.1:n.3221-13_3221-12delinsCT
XM_005245812.1:c.3209-13_3209-12delinsCT	XP_005245869.1:n.3209-13_3209-12delinsCT
XM_005245813.1:c.3176-13_3176-12delinsCT	XP_005245870.1:n.3176-13_3176-12delinsCT
XM_005245815.1:c.3119-13_3119-12delinsCT	XP_005245872.1:n.3119-13_3119-12delinsCT
XM_006710512.1:c.3218-13_3218-12delinsCT	XP_006710575.1:n.3218-13_3218-12delinsCT
XM_006710513.1:c.3194-13_3194-12delinsCT	XP_006710576.1:n.3194-13_3194-12delinsCT
XM_011541128.1:c.3221-13_3221-12delinsCT	XP_011539430.1:n.3221-13_3221-12delinsCT
XM_011541129.1:c.3029-13_3029-12delinsCT	XP_011539431.1:n.3029-13_3029-12delinsCT
XM_017000844.1:c.3391-13_3391-12delinsCT	XP_016856333.1:n.3391-13_3391-12delinsCT
XM_017000845.1:c.3388-13_3388-12delinsCT	XP_016856334.1:n.3388-13_3388-12delinsCT
XM_017000846.1:c.3364-13_3364-12delinsCT	XP_016856335.1:n.3364-13_3364-12delinsCT
XM_017000847.1:c.3361-13_3361-12delinsCT	XP_016856336.1:n.3361-13_3361-12delinsCT
XM_017000848.1:c.3289-13_3289-12delinsCT	XP_016856337.1:n.3289-13_3289-12delinsCT
XM_017000849.1:c.3274-13_3274-12delinsCT	XP_016856338.1:n.3274-13_3274-12delinsCT
XM_017000850.1:c.3199-13_3199-12delinsCT	XP_016856339.1:n.3199-13_3199-12delinsCT
NM_022089.4:c.3406-13_3406-12delinsCT MANE Select	NP_071372.1:n.3406-13_3406-12delinsCT
NM_001141973.3:c.3391-13_3391-12delinsCT	NP_001135445.1:n.3391-13_3391-12delinsCT
NM_001141974.3:c.3104-13_3104-12delinsCT	NP_001135446.1:n.3104-13_3104-12delinsCT