Canonical Allele Identifier: CA338231331

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17312635G>A (hg19) ; chr1:g.16986140G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986140G>A , CM000663.2:g.16986140G>A	GRCh38
NC_000001.10:g.17312635G>A , CM000663.1:g.17312635G>A	GRCh37
NC_000001.9:g.17185222G>A	NCBI36
NG_009054.1:g.30789C>T
NG_029688.1:g.447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.*81C>T MANE Select	ENSP00000327214.8:n.*81C>T
ENST00000326735.12:c.*81C>T	ENSP00000327214.8:n.*81C>T
ENST00000341676.9:c.3322C>T	ENSP00000341115.5:p.Pro1108Ser
ENST00000452699.5:c.*81C>T	ENSP00000413307.1:n.*81C>T
ENST00000466561.1:n.1670C>T
ENST00000502418.1:c.1042C>T	ENSP00000423065.1:p.Pro348Ser
NM_001141973.2:c.*81C>T	NP_001135445.1:n.*81C>T
NM_001141974.2:c.3322C>T	NP_001135446.1:p.Pro1108Ser
NM_022089.3:c.*81C>T	NP_071372.1:n.*81C>T
XM_005245809.1:c.3454C>T	XP_005245866.1:p.Pro1152Ser
XM_005245810.1:c.3451C>T	XP_005245867.1:p.Pro1151Ser
XM_005245811.1:c.3439C>T	XP_005245868.1:p.Pro1147Ser
XM_005245812.1:c.3427C>T	XP_005245869.1:p.Pro1143Ser
XM_005245813.1:c.3394C>T	XP_005245870.1:p.Pro1132Ser
XM_005245815.1:c.3337C>T	XP_005245872.1:p.Pro1113Ser
XM_006710512.1:c.3436C>T	XP_006710575.1:p.Pro1146Ser
XM_006710513.1:c.3412C>T	XP_006710576.1:p.Pro1138Ser
XM_011541128.1:c.3439C>T	XP_011539430.1:p.Pro1147Ser
XM_011541129.1:c.3247C>T	XP_011539431.1:p.Pro1083Ser
XM_017000844.1:c.*81C>T	XP_016856333.1:n.*81C>T
XM_017000845.1:c.*81C>T	XP_016856334.1:n.*81C>T
XM_017000846.1:c.*81C>T	XP_016856335.1:n.*81C>T
XM_017000847.1:c.*81C>T	XP_016856336.1:n.*81C>T
XM_017000848.1:c.*81C>T	XP_016856337.1:n.*81C>T
XM_017000849.1:c.*81C>T	XP_016856338.1:n.*81C>T
XM_017000850.1:c.*81C>T	XP_016856339.1:n.*81C>T
NM_022089.4:c.*81C>T MANE Select	NP_071372.1:n.*81C>T
NM_001141973.3:c.*81C>T	NP_001135445.1:n.*81C>T
NM_001141974.3:c.3322C>T	NP_001135446.1:p.Pro1108Ser