Canonical Allele Identifier: CA338254818
Gene: ATP13A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16996472A>G , CM000663.2:g.16996472A>G GRCh38
NC_000001.10:g.17322967A>G , CM000663.1:g.17322967A>G GRCh37
NC_000001.9:g.17195554A>G NCBI36
NG_009054.1:g.20457T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326735.13:c.1220T>C MANE Select ENSP00000327214.8:p.Leu407Pro
ENST00000326735.12:c.1220T>C ENSP00000327214.8:p.Leu407Pro
ENST00000341676.9:c.1205T>C ENSP00000341115.5:p.Leu402Pro
ENST00000452699.5:c.1205T>C ENSP00000413307.1:p.Leu402Pro
ENST00000463860.5:n.828T>C
ENST00000502860.1:n.335-172T>C
ENST00000506174.5:c.362T>C ENSP00000424393.1:p.Leu121Pro
ENST00000509392.1:n.223T>C
ENST00000617114.4:c.335-172T>C ENSP00000478781.1:n.335-172T>C
NM_001141973.2:c.1205T>C NP_001135445.1:p.Leu402Pro
NM_001141974.2:c.1205T>C NP_001135446.1:p.Leu402Pro
NM_022089.3:c.1220T>C NP_071372.1:p.Leu407Pro
XM_005245809.1:c.1220T>C XP_005245866.1:p.Leu407Pro
XM_005245810.1:c.1217T>C XP_005245867.1:p.Leu406Pro
XM_005245811.1:c.1205T>C XP_005245868.1:p.Leu402Pro
XM_005245812.1:c.1193T>C XP_005245869.1:p.Leu398Pro
XM_005245813.1:c.1220T>C XP_005245870.1:p.Leu407Pro
XM_005245815.1:c.1220T>C XP_005245872.1:p.Leu407Pro
XM_006710512.1:c.1202T>C XP_006710575.1:p.Leu401Pro
XM_006710513.1:c.1178T>C XP_006710576.1:p.Leu393Pro
XM_011541128.1:c.1220T>C XP_011539430.1:p.Leu407Pro
XM_011541129.1:c.1220T>C XP_011539431.1:p.Leu407Pro
XM_017000844.1:c.1220T>C XP_016856333.1:p.Leu407Pro
XM_017000845.1:c.1202T>C XP_016856334.1:p.Leu401Pro
XM_017000846.1:c.1178T>C XP_016856335.1:p.Leu393Pro
XM_017000847.1:c.1190T>C XP_016856336.1:p.Leu397Pro
XM_017000848.1:c.1220T>C XP_016856337.1:p.Leu407Pro
XM_017000849.1:c.1205T>C XP_016856338.1:p.Leu402Pro
XM_017000850.1:c.1220T>C XP_016856339.1:p.Leu407Pro
NM_022089.4:c.1220T>C MANE Select NP_071372.1:p.Leu407Pro
NM_001141973.3:c.1205T>C NP_001135445.1:p.Leu402Pro
NM_001141974.3:c.1205T>C NP_001135446.1:p.Leu402Pro