Canonical Allele Identifier: CA636529

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986554G>A , CM000663.2:g.16986554G>A	GRCh38
NC_000001.10:g.17313049G>A , CM000663.1:g.17313049G>A	GRCh37
NC_000001.9:g.17185636G>A	NCBI36
NG_009054.1:g.30375C>T
NG_029688.1:g.33C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022089.4:c.3314C>T MANE Select	NP_071372.1:p.Pro1105Leu
ENST00000326735.13:c.3314C>T MANE Select	ENSP00000327214.8:p.Pro1105Leu
NM_001141973.2:c.3299C>T	NP_001135445.1:p.Pro1100Leu
NM_001141973.3:c.3299C>T	NP_001135445.1:p.Pro1100Leu
NM_001141974.2:c.3104-196C>T	NP_001135446.1:n.3104-196C>T
NM_001141974.3:c.3104-196C>T	NP_001135446.1:n.3104-196C>T
NM_022089.3:c.3314C>T	NP_071372.1:p.Pro1105Leu
ENST00000326735.12:c.3314C>T	ENSP00000327214.8:p.Pro1105Leu
ENST00000341676.9:c.3104-196C>T	ENSP00000341115.5:n.3104-196C>T
ENST00000452699.5:c.3299C>T	ENSP00000413307.1:p.Pro1100Leu
ENST00000466561.1:n.1360C>T
ENST00000502418.1:c.824-196C>T	ENSP00000423065.1:n.824-196C>T
XM_005245809.1:c.3236-196C>T	XP_005245866.1:n.3236-196C>T
XM_005245810.1:c.3233-196C>T	XP_005245867.1:n.3233-196C>T
XM_005245811.1:c.3221-196C>T	XP_005245868.1:n.3221-196C>T
XM_005245812.1:c.3209-196C>T	XP_005245869.1:n.3209-196C>T
XM_005245813.1:c.3176-196C>T	XP_005245870.1:n.3176-196C>T
XM_005245815.1:c.3119-196C>T	XP_005245872.1:n.3119-196C>T
XM_006710512.1:c.3218-196C>T	XP_006710575.1:n.3218-196C>T
XM_006710513.1:c.3194-196C>T	XP_006710576.1:n.3194-196C>T
XM_011541128.1:c.3221-196C>T	XP_011539430.1:n.3221-196C>T
XM_011541129.1:c.3029-196C>T	XP_011539431.1:n.3029-196C>T
XM_017000844.1:c.3299C>T	XP_016856333.1:p.Pro1100Leu
XM_017000845.1:c.3296C>T	XP_016856334.1:p.Pro1099Leu
XM_017000846.1:c.3272C>T	XP_016856335.1:p.Pro1091Leu
XM_017000847.1:c.3269C>T	XP_016856336.1:p.Pro1090Leu
XM_017000848.1:c.3197C>T	XP_016856337.1:p.Pro1066Leu
XM_017000849.1:c.3182C>T	XP_016856338.1:p.Pro1061Leu
XM_017000850.1:c.3107C>T	XP_016856339.1:p.Pro1036Leu