Canonical Allele Identifier: CA2574234955
Gene: ATP13A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16986515_16986517dup , CM000663.2:g.16986515_16986517dup GRCh38
NC_000001.10:g.17313010_17313012dup , CM000663.1:g.17313010_17313012dup GRCh37
NC_000001.9:g.17185597_17185599dup NCBI36
NG_009054.1:g.30422_30424dup
NG_029688.1:g.80_82dup

Transcript Alleles

HGVS Amino-acid change
ENST00000326735.13:c.3361_3363dup MANE Select ENSP00000327214.8:p.Leu1121_Gly1122insLeu...
ENST00000326735.12:c.3361_3363dup ENSP00000327214.8:p.Leu1121_Gly1122insLeu...
ENST00000341676.9:c.3104-149_3104-147dup ENSP00000341115.5:n.3104-149_3104-147dup
ENST00000452699.5:c.3346_3348dup ENSP00000413307.1:p.Leu1116_Gly1117insLeu...
ENST00000466561.1:n.1407_1409dup
ENST00000502418.1:c.824-149_824-147dup ENSP00000423065.1:n.824-149_824-147dup
NM_001141973.2:c.3346_3348dup NP_001135445.1:p.Leu1116_Gly1117insLeu
NM_001141974.2:c.3104-149_3104-147dup NP_001135446.1:n.3104-149_3104-147dup
NM_022089.3:c.3361_3363dup NP_071372.1:p.Leu1121_Gly1122insLeu
XM_005245809.1:c.3236-149_3236-147dup XP_005245866.1:n.3236-149_3236-147dup
XM_005245810.1:c.3233-149_3233-147dup XP_005245867.1:n.3233-149_3233-147dup
XM_005245811.1:c.3221-149_3221-147dup XP_005245868.1:n.3221-149_3221-147dup
XM_005245812.1:c.3209-149_3209-147dup XP_005245869.1:n.3209-149_3209-147dup
XM_005245813.1:c.3176-149_3176-147dup XP_005245870.1:n.3176-149_3176-147dup
XM_005245815.1:c.3119-149_3119-147dup XP_005245872.1:n.3119-149_3119-147dup
XM_006710512.1:c.3218-149_3218-147dup XP_006710575.1:n.3218-149_3218-147dup
XM_006710513.1:c.3194-149_3194-147dup XP_006710576.1:n.3194-149_3194-147dup
XM_011541128.1:c.3221-149_3221-147dup XP_011539430.1:n.3221-149_3221-147dup
XM_011541129.1:c.3029-149_3029-147dup XP_011539431.1:n.3029-149_3029-147dup
XM_017000844.1:c.3346_3348dup XP_016856333.1:p.Leu1116_Gly1117insLeu
XM_017000845.1:c.3343_3345dup XP_016856334.1:p.Leu1115_Gly1116insLeu
XM_017000846.1:c.3319_3321dup XP_016856335.1:p.Leu1107_Gly1108insLeu
XM_017000847.1:c.3316_3318dup XP_016856336.1:p.Leu1106_Gly1107insLeu
XM_017000848.1:c.3244_3246dup XP_016856337.1:p.Leu1082_Gly1083insLeu
XM_017000849.1:c.3229_3231dup XP_016856338.1:p.Leu1077_Gly1078insLeu
XM_017000850.1:c.3154_3156dup XP_016856339.1:p.Leu1052_Gly1053insLeu
NM_022089.4:c.3361_3363dup MANE Select NP_071372.1:p.Leu1121_Gly1122insLeu
NM_001141973.3:c.3346_3348dup NP_001135445.1:p.Leu1116_Gly1117insLeu
NM_001141974.3:c.3104-149_3104-147dup NP_001135446.1:n.3104-149_3104-147dup