Canonical Allele Identifier: CA1189926715

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113847041_113847042delinsAT , CM000663.2:g.113847041_113847042delinsAT	GRCh38
NC_000001.10:g.114389663_114389664delinsAT , CM000663.1:g.114389663_114389664delinsAT	GRCh37
NC_000001.9:g.114191186_114191187delinsAT	NCBI36
NG_011432.1:g.29712_29713delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.915+1498_915+1499delinsAT (PTPN22) MANE Select	ENSP00000352833.5:n.915+1498_915+1499delinsAT
ENST00000359785.9:c.915+1498_915+1499delinsAT (PTPN22)	ENSP00000352833.5:n.915+1498_915+1499delinsAT
ENST00000420377.6:c.915+1498_915+1499delinsAT (PTPN22)	ENSP00000388229.2:n.915+1498_915+1499delinsAT
ENST00000460620.5:c.468+9340_468+9341delinsAT (PTPN22)	ENSP00000433141.1:n.468+9340_468+9341delinsAT
ENST00000484147.5:n.956+1498_956+1499delinsAT (PTPN22)
ENST00000525799.1:c.534+1498_534+1499delinsAT (PTPN22)	ENSP00000432674.1:n.534+1498_534+1499delinsAT
ENST00000528414.5:c.750+7429_750+7430delinsAT (PTPN22)	ENSP00000435176.1:n.750+7429_750+7430delinsAT
ENST00000532224.5:c.*193+1498_*193+1499delinsAT (PTPN22)	ENSP00000431249.1:n.*193+1498_*193+1499delinsAT
ENST00000538253.5:c.843+1498_843+1499delinsAT (PTPN22)	ENSP00000439372.2:n.843+1498_843+1499delinsAT
NM_001193431.1:c.915+1498_915+1499delinsAT (PTPN22)	NP_001180360.1:n.915+1498_915+1499delinsAT
NM_001193431.2:c.915+1498_915+1499delinsAT (PTPN22)	NP_001180360.1:n.915+1498_915+1499delinsAT
NM_001308297.1:c.843+1498_843+1499delinsAT (PTPN22)	NP_001295226.1:n.843+1498_843+1499delinsAT
NM_012411.4:c.750+7429_750+7430delinsAT (PTPN22)	NP_036543.4:n.750+7429_750+7430delinsAT
NM_012411.5:c.750+7429_750+7430delinsAT (PTPN22)	NP_036543.4:n.750+7429_750+7430delinsAT
NM_015967.5:c.915+1498_915+1499delinsAT (PTPN22)	NP_057051.3:n.915+1498_915+1499delinsAT
NM_015967.6:c.915+1498_915+1499delinsAT (PTPN22)	NP_057051.3:n.915+1498_915+1499delinsAT
NR_125965.1:n.414+31569_414+31570delinsAT (AP4B1-AS1)
XM_011541221.1:c.837+1498_837+1499delinsAT (PTPN22)	XP_011539523.1:n.837+1498_837+1499delinsAT
XM_011541222.1:c.915+1498_915+1499delinsAT (PTPN22)	XP_011539524.1:n.915+1498_915+1499delinsAT
XM_011541223.1:c.915+1498_915+1499delinsAT (PTPN22)	XP_011539525.1:n.915+1498_915+1499delinsAT
XM_011541224.1:c.471+1498_471+1499delinsAT (PTPN22)	XP_011539526.1:n.471+1498_471+1499delinsAT
XM_011541225.1:c.843+1498_843+1499delinsAT (PTPN22)	XP_011539527.1:n.843+1498_843+1499delinsAT
XM_011541223.2:c.915+1498_915+1499delinsAT (PTPN22)	XP_011539525.1:n.915+1498_915+1499delinsAT
XM_011541225.2:c.843+1498_843+1499delinsAT (PTPN22)	XP_011539527.1:n.843+1498_843+1499delinsAT
XM_017001004.1:c.915+1498_915+1499delinsAT (PTPN22)	XP_016856493.1:n.915+1498_915+1499delinsAT
XM_017001005.2:c.570+1498_570+1499delinsAT (PTPN22)	XP_016856494.1:n.570+1498_570+1499delinsAT
XM_017001006.1:c.915+1498_915+1499delinsAT (PTPN22)	XP_016856495.1:n.915+1498_915+1499delinsAT
NM_015967.7:c.915+1498_915+1499delinsAT (PTPN22)	NP_057051.3:n.915+1498_915+1499delinsAT
NM_015967.8:c.915+1498_915+1499delinsAT (PTPN22) MANE Select	NP_057051.4:n.915+1498_915+1499delinsAT