Canonical Allele Identifier: CA1189920225

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113829918_113829919delinsGA , CM000663.2:g.113829918_113829919delinsGA	GRCh38
NC_000001.10:g.114372540_114372541delinsGA , CM000663.1:g.114372540_114372541delinsGA	GRCh37
NC_000001.9:g.114174063_114174064delinsGA	NCBI36
NG_011432.1:g.46835_46836delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.2134+30_2134+31delinsTC (PTPN22) MANE Select	ENSP00000352833.5:n.2134+30_2134+31delinsTC
ENST00000359785.9:c.2134+30_2134+31delinsTC (PTPN22)	ENSP00000352833.5:n.2134+30_2134+31delinsTC
ENST00000420377.6:c.2134+30_2134+31delinsTC (PTPN22)	ENSP00000388229.2:n.2134+30_2134+31delinsTC
ENST00000460620.5:c.469-10265_469-10264delinsTC (PTPN22)	ENSP00000433141.1:n.469-10265_469-10264delinsTC
ENST00000525799.1:c.1753+30_1753+31delinsTC (PTPN22)	ENSP00000432674.1:n.1753+30_1753+31delinsTC
ENST00000528414.5:c.1969+30_1969+31delinsTC (PTPN22)	ENSP00000435176.1:n.1969+30_1969+31delinsTC
ENST00000532224.5:c.*1412+30_*1412+31delinsTC (PTPN22)	ENSP00000431249.1:n.*1412+30_*1412+31delinsTC
ENST00000538253.5:c.2062+30_2062+31delinsTC (PTPN22)	ENSP00000439372.2:n.2062+30_2062+31delinsTC
NM_001193431.1:c.2050+30_2050+31delinsTC (PTPN22)	NP_001180360.1:n.2050+30_2050+31delinsTC
NM_001193431.2:c.2050+30_2050+31delinsTC (PTPN22)	NP_001180360.1:n.2050+30_2050+31delinsTC
NM_001308297.1:c.2062+30_2062+31delinsTC (PTPN22)	NP_001295226.1:n.2062+30_2062+31delinsTC
NM_012411.4:c.1969+30_1969+31delinsTC (PTPN22)	NP_036543.4:n.1969+30_1969+31delinsTC
NM_012411.5:c.1969+30_1969+31delinsTC (PTPN22)	NP_036543.4:n.1969+30_1969+31delinsTC
NM_015967.5:c.2134+30_2134+31delinsTC (PTPN22)	NP_057051.3:n.2134+30_2134+31delinsTC
NM_015967.6:c.2134+30_2134+31delinsTC (PTPN22)	NP_057051.3:n.2134+30_2134+31delinsTC
NR_125965.1:n.414+14446_414+14447delinsGA (AP4B1-AS1)
XM_011541221.1:c.2056+30_2056+31delinsTC (PTPN22)	XP_011539523.1:n.2056+30_2056+31delinsTC
XM_011541222.1:c.2134+30_2134+31delinsTC (PTPN22)	XP_011539524.1:n.2134+30_2134+31delinsTC
XM_011541224.1:c.1690+30_1690+31delinsTC (PTPN22)	XP_011539526.1:n.1690+30_1690+31delinsTC
XM_011541225.1:c.2062+30_2062+31delinsTC (PTPN22)	XP_011539527.1:n.2062+30_2062+31delinsTC
XM_011541225.2:c.2062+30_2062+31delinsTC (PTPN22)	XP_011539527.1:n.2062+30_2062+31delinsTC
XM_017001004.1:c.2134+30_2134+31delinsTC (PTPN22)	XP_016856493.1:n.2134+30_2134+31delinsTC
XM_017001005.2:c.1789+30_1789+31delinsTC (PTPN22)	XP_016856494.1:n.1789+30_1789+31delinsTC
NM_015967.7:c.2134+30_2134+31delinsTC (PTPN22)	NP_057051.3:n.2134+30_2134+31delinsTC
NM_015967.8:c.2134+30_2134+31delinsTC (PTPN22) MANE Select	NP_057051.4:n.2134+30_2134+31delinsTC