Canonical Allele Identifier: CA636657

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16987164G>A , CM000663.2:g.16987164G>A	GRCh38
NC_000001.10:g.17313659G>A , CM000663.1:g.17313659G>A	GRCh37
NC_000001.9:g.17186246G>A	NCBI36
NG_009054.1:g.29765C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022089.4:c.2965C>T MANE Select	NP_071372.1:p.Arg989Trp
ENST00000326735.13:c.2965C>T MANE Select	ENSP00000327214.8:p.Arg989Trp
NM_001141973.2:c.2950C>T	NP_001135445.1:p.Arg984Trp
NM_001141973.3:c.2950C>T	NP_001135445.1:p.Arg984Trp
NM_001141974.2:c.2833C>T	NP_001135446.1:p.Arg945Trp
NM_001141974.3:c.2833C>T	NP_001135446.1:p.Arg945Trp
NM_022089.3:c.2965C>T	NP_071372.1:p.Arg989Trp
ENST00000326735.12:c.2965C>T	ENSP00000327214.8:p.Arg989Trp
ENST00000341676.9:c.2833C>T	ENSP00000341115.5:p.Arg945Trp
ENST00000452699.5:c.2950C>T	ENSP00000413307.1:p.Arg984Trp
ENST00000466561.1:n.839C>T
ENST00000502418.1:c.553C>T	ENSP00000423065.1:p.Arg185Trp
XM_005245809.1:c.2965C>T	XP_005245866.1:p.Arg989Trp
XM_005245810.1:c.2962C>T	XP_005245867.1:p.Arg988Trp
XM_005245811.1:c.2950C>T	XP_005245868.1:p.Arg984Trp
XM_005245812.1:c.2938C>T	XP_005245869.1:p.Arg980Trp
XM_005245813.1:c.2905C>T	XP_005245870.1:p.Arg969Trp
XM_005245815.1:c.2848C>T	XP_005245872.1:p.Arg950Trp
XM_006710512.1:c.2947C>T	XP_006710575.1:p.Arg983Trp
XM_006710513.1:c.2923C>T	XP_006710576.1:p.Arg975Trp
XM_011541128.1:c.2950C>T	XP_011539430.1:p.Arg984Trp
XM_011541129.1:c.2758C>T	XP_011539431.1:p.Arg920Trp
XM_017000844.1:c.2950C>T	XP_016856333.1:p.Arg984Trp
XM_017000845.1:c.2947C>T	XP_016856334.1:p.Arg983Trp
XM_017000846.1:c.2923C>T	XP_016856335.1:p.Arg975Trp
XM_017000847.1:c.2920C>T	XP_016856336.1:p.Arg974Trp
XM_017000848.1:c.2848C>T	XP_016856337.1:p.Arg950Trp
XM_017000849.1:c.2833C>T	XP_016856338.1:p.Arg945Trp
XM_017000850.1:c.2758C>T	XP_016856339.1:p.Arg920Trp