Canonical Allele Identifier: CA28972843
Gene: PTPN22 HGNC NCBI
AP4B1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs146706560

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113846972_113846973insG , CM000663.2:g.113846972_113846973insG GRCh38
NC_000001.10:g.114389594_114389595insG , CM000663.1:g.114389594_114389595insG GRCh37
NC_000001.9:g.114191117_114191118insG NCBI36
NG_011432.1:g.29781_29782insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000359785.10:c.915+1567_915+1568insC (PTPN22) MANE Select ENSP00000352833.5:n.915+1567_915+1568insC
ENST00000359785.9:c.915+1567_915+1568insC (PTPN22) ENSP00000352833.5:n.915+1567_915+1568insC
ENST00000420377.6:c.915+1567_915+1568insC (PTPN22) ENSP00000388229.2:n.915+1567_915+1568insC
ENST00000460620.5:c.468+9409_468+9410insC (PTPN22) ENSP00000433141.1:n.468+9409_468+9410insC
ENST00000484147.5:n.956+1567_956+1568insC (PTPN22)
ENST00000525799.1:c.534+1567_534+1568insC (PTPN22) ENSP00000432674.1:n.534+1567_534+1568insC
ENST00000528414.5:c.750+7498_750+7499insC (PTPN22) ENSP00000435176.1:n.750+7498_750+7499insC
ENST00000532224.5:c.*193+1567_*193+1568insC (PTPN22) ENSP00000431249.1:n.*193+1567_*193+1568insC
ENST00000538253.5:c.843+1567_843+1568insC (PTPN22) ENSP00000439372.2:n.843+1567_843+1568insC
NM_001193431.1:c.915+1567_915+1568insC (PTPN22) NP_001180360.1:n.915+1567_915+1568insC
NM_001193431.2:c.915+1567_915+1568insC (PTPN22) NP_001180360.1:n.915+1567_915+1568insC
NM_001308297.1:c.843+1567_843+1568insC (PTPN22) NP_001295226.1:n.843+1567_843+1568insC
NM_012411.4:c.750+7498_750+7499insC (PTPN22) NP_036543.4:n.750+7498_750+7499insC
NM_012411.5:c.750+7498_750+7499insC (PTPN22) NP_036543.4:n.750+7498_750+7499insC
NM_015967.5:c.915+1567_915+1568insC (PTPN22) NP_057051.3:n.915+1567_915+1568insC
NM_015967.6:c.915+1567_915+1568insC (PTPN22) NP_057051.3:n.915+1567_915+1568insC
NR_125965.1:n.414+31500_414+31501insG (AP4B1-AS1)
XM_011541221.1:c.837+1567_837+1568insC (PTPN22) XP_011539523.1:n.837+1567_837+1568insC
XM_011541222.1:c.915+1567_915+1568insC (PTPN22) XP_011539524.1:n.915+1567_915+1568insC
XM_011541223.1:c.915+1567_915+1568insC (PTPN22) XP_011539525.1:n.915+1567_915+1568insC
XM_011541224.1:c.471+1567_471+1568insC (PTPN22) XP_011539526.1:n.471+1567_471+1568insC
XM_011541225.1:c.843+1567_843+1568insC (PTPN22) XP_011539527.1:n.843+1567_843+1568insC
XM_011541223.2:c.915+1567_915+1568insC (PTPN22) XP_011539525.1:n.915+1567_915+1568insC
XM_011541225.2:c.843+1567_843+1568insC (PTPN22) XP_011539527.1:n.843+1567_843+1568insC
XM_017001004.1:c.915+1567_915+1568insC (PTPN22) XP_016856493.1:n.915+1567_915+1568insC
XM_017001005.2:c.570+1567_570+1568insC (PTPN22) XP_016856494.1:n.570+1567_570+1568insC
XM_017001006.1:c.915+1567_915+1568insC (PTPN22) XP_016856495.1:n.915+1567_915+1568insC
NM_015967.7:c.915+1567_915+1568insC (PTPN22) NP_057051.3:n.915+1567_915+1568insC
NM_015967.8:c.915+1567_915+1568insC (PTPN22) MANE Select NP_057051.4:n.915+1567_915+1568insC