Canonical Allele Identifier: CA1156049654

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986381_16986383delinsCAG , CM000663.2:g.16986381_16986383delinsCAG	GRCh38
NC_000001.10:g.17312876_17312878delinsCAG , CM000663.1:g.17312876_17312878delinsCAG	GRCh37
NC_000001.9:g.17185463_17185465delinsCAG	NCBI36
NG_009054.1:g.30546_30548delinsCTG
NG_029688.1:g.204_206delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.3406-25_3406-23delinsCTG MANE Select	ENSP00000327214.8:n.3406-25_3406-23delinsCTG
ENST00000326735.12:c.3406-25_3406-23delinsCTG	ENSP00000327214.8:n.3406-25_3406-23delinsCTG
ENST00000341676.9:c.3104-25_3104-23delinsCTG	ENSP00000341115.5:n.3104-25_3104-23delinsCTG
ENST00000452699.5:c.3391-25_3391-23delinsCTG	ENSP00000413307.1:n.3391-25_3391-23delinsCTG
ENST00000466561.1:n.1452-25_1452-23delinsCTG
ENST00000502418.1:c.824-25_824-23delinsCTG	ENSP00000423065.1:n.824-25_824-23delinsCTG
NM_001141973.2:c.3391-25_3391-23delinsCTG	NP_001135445.1:n.3391-25_3391-23delinsCTG
NM_001141974.2:c.3104-25_3104-23delinsCTG	NP_001135446.1:n.3104-25_3104-23delinsCTG
NM_022089.3:c.3406-25_3406-23delinsCTG	NP_071372.1:n.3406-25_3406-23delinsCTG
XM_005245809.1:c.3236-25_3236-23delinsCTG	XP_005245866.1:n.3236-25_3236-23delinsCTG
XM_005245810.1:c.3233-25_3233-23delinsCTG	XP_005245867.1:n.3233-25_3233-23delinsCTG
XM_005245811.1:c.3221-25_3221-23delinsCTG	XP_005245868.1:n.3221-25_3221-23delinsCTG
XM_005245812.1:c.3209-25_3209-23delinsCTG	XP_005245869.1:n.3209-25_3209-23delinsCTG
XM_005245813.1:c.3176-25_3176-23delinsCTG	XP_005245870.1:n.3176-25_3176-23delinsCTG
XM_005245815.1:c.3119-25_3119-23delinsCTG	XP_005245872.1:n.3119-25_3119-23delinsCTG
XM_006710512.1:c.3218-25_3218-23delinsCTG	XP_006710575.1:n.3218-25_3218-23delinsCTG
XM_006710513.1:c.3194-25_3194-23delinsCTG	XP_006710576.1:n.3194-25_3194-23delinsCTG
XM_011541128.1:c.3221-25_3221-23delinsCTG	XP_011539430.1:n.3221-25_3221-23delinsCTG
XM_011541129.1:c.3029-25_3029-23delinsCTG	XP_011539431.1:n.3029-25_3029-23delinsCTG
XM_017000844.1:c.3391-25_3391-23delinsCTG	XP_016856333.1:n.3391-25_3391-23delinsCTG
XM_017000845.1:c.3388-25_3388-23delinsCTG	XP_016856334.1:n.3388-25_3388-23delinsCTG
XM_017000846.1:c.3364-25_3364-23delinsCTG	XP_016856335.1:n.3364-25_3364-23delinsCTG
XM_017000847.1:c.3361-25_3361-23delinsCTG	XP_016856336.1:n.3361-25_3361-23delinsCTG
XM_017000848.1:c.3289-25_3289-23delinsCTG	XP_016856337.1:n.3289-25_3289-23delinsCTG
XM_017000849.1:c.3274-25_3274-23delinsCTG	XP_016856338.1:n.3274-25_3274-23delinsCTG
XM_017000850.1:c.3199-25_3199-23delinsCTG	XP_016856339.1:n.3199-25_3199-23delinsCTG
NM_022089.4:c.3406-25_3406-23delinsCTG MANE Select	NP_071372.1:n.3406-25_3406-23delinsCTG
NM_001141973.3:c.3391-25_3391-23delinsCTG	NP_001135445.1:n.3391-25_3391-23delinsCTG
NM_001141974.3:c.3104-25_3104-23delinsCTG	NP_001135446.1:n.3104-25_3104-23delinsCTG