Canonical Allele Identifier: CA1148224177

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16989739A= , CM000663.2:g.16989739A=	GRCh38
NC_000001.10:g.17316234A= , CM000663.1:g.17316234A=	GRCh37
NC_000001.9:g.17188821A=	NCBI36
NG_009054.1:g.27190T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.2561T= MANE Select	ENSP00000327214.8:p.Met854=
ENST00000326735.12:c.2561T=	ENSP00000327214.8:p.Met854=
ENST00000341676.9:c.2429T=	ENSP00000341115.5:p.Met810=
ENST00000452699.5:c.2546T=	ENSP00000413307.1:p.Met849=
ENST00000466561.1:n.435T=
ENST00000502418.1:c.149T=	ENSP00000423065.1:p.Met50=
NM_001141973.2:c.2546T=	NP_001135445.1:p.Met849=
NM_001141974.2:c.2429T=	NP_001135446.1:p.Met810=
NM_022089.3:c.2561T=	NP_071372.1:p.Met854=
XM_005245809.1:c.2561T=	XP_005245866.1:p.Met854=
XM_005245810.1:c.2558T=	XP_005245867.1:p.Met853=
XM_005245811.1:c.2546T=	XP_005245868.1:p.Met849=
XM_005245812.1:c.2534T=	XP_005245869.1:p.Met845=
XM_005245813.1:c.2501T=	XP_005245870.1:p.Met834=
XM_005245815.1:c.2444T=	XP_005245872.1:p.Met815=
XM_006710512.1:c.2543T=	XP_006710575.1:p.Met848=
XM_006710513.1:c.2519T=	XP_006710576.1:p.Met840=
XM_011541128.1:c.2546T=	XP_011539430.1:p.Met849=
XM_011541129.1:c.2354T=	XP_011539431.1:p.Met785=
XM_017000844.1:c.2546T=	XP_016856333.1:p.Met849=
XM_017000845.1:c.2543T=	XP_016856334.1:p.Met848=
XM_017000846.1:c.2519T=	XP_016856335.1:p.Met840=
XM_017000847.1:c.2516T=	XP_016856336.1:p.Met839=
XM_017000848.1:c.2444T=	XP_016856337.1:p.Met815=
XM_017000849.1:c.2429T=	XP_016856338.1:p.Met810=
XM_017000850.1:c.2354T=	XP_016856339.1:p.Met785=
NM_022089.4:c.2561T= MANE Select	NP_071372.1:p.Met854=
NM_001141973.3:c.2546T=	NP_001135445.1:p.Met849=
NM_001141974.3:c.2429T=	NP_001135446.1:p.Met810=