Canonical Allele Identifier: CA2535535368

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113829928_113829929insCAAAATCCTTTATTTATAA , CM000663.2:g.113829928_113829929insCAAAATCCTTTATTTATAA	GRCh38
NC_000001.10:g.114372550_114372551insCAAAATCCTTTATTTATAA , CM000663.1:g.114372550_114372551insCAAAATCCTTTATTTATAA	GRCh37
NC_000001.9:g.114174073_114174074insCAAAATCCTTTATTTATAA	NCBI36
NG_011432.1:g.46826_46827insTATAAATAAAGGATTTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22) MANE Select	ENSP00000352833.5:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
ENST00000359785.9:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22)	ENSP00000352833.5:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
ENST00000420377.6:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22)	ENSP00000388229.2:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
ENST00000460620.5:c.469-10274_469-10273insTATAAATAAAGGATTTTGT (PTPN22)	ENSP00000433141.1:n.469-10274_469-10273insTATAAATAAAGGATTTTGT...
ENST00000525799.1:c.1753+21_1753+22insTATAAATAAAGGATTTTGT (PTPN22)	ENSP00000432674.1:n.1753+21_1753+22insTATAAATAAAGGATTTTGT
ENST00000528414.5:c.1969+21_1969+22insTATAAATAAAGGATTTTGT (PTPN22)	ENSP00000435176.1:n.1969+21_1969+22insTATAAATAAAGGATTTTGT
ENST00000532224.5:c.*1412+21_*1412+22insTATAAATAAAGGATTTTGT (PTPN22)	ENSP00000431249.1:n.*1412+21_*1412+22insTATAAATAAAGGATTTTGT
ENST00000538253.5:c.2062+21_2062+22insTATAAATAAAGGATTTTGT (PTPN22)	ENSP00000439372.2:n.2062+21_2062+22insTATAAATAAAGGATTTTGT
NM_001193431.1:c.2050+21_2050+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_001180360.1:n.2050+21_2050+22insTATAAATAAAGGATTTTGT
NM_001193431.2:c.2050+21_2050+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_001180360.1:n.2050+21_2050+22insTATAAATAAAGGATTTTGT
NM_001308297.1:c.2062+21_2062+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_001295226.1:n.2062+21_2062+22insTATAAATAAAGGATTTTGT
NM_012411.4:c.1969+21_1969+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_036543.4:n.1969+21_1969+22insTATAAATAAAGGATTTTGT
NM_012411.5:c.1969+21_1969+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_036543.4:n.1969+21_1969+22insTATAAATAAAGGATTTTGT
NM_015967.5:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_057051.3:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
NM_015967.6:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_057051.3:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
NR_125965.1:n.414+14456_414+14457insCAAAATCCTTTATTTATAA (AP4B1-AS1)
XM_011541221.1:c.2056+21_2056+22insTATAAATAAAGGATTTTGT (PTPN22)	XP_011539523.1:n.2056+21_2056+22insTATAAATAAAGGATTTTGT
XM_011541222.1:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22)	XP_011539524.1:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
XM_011541224.1:c.1690+21_1690+22insTATAAATAAAGGATTTTGT (PTPN22)	XP_011539526.1:n.1690+21_1690+22insTATAAATAAAGGATTTTGT
XM_011541225.1:c.2062+21_2062+22insTATAAATAAAGGATTTTGT (PTPN22)	XP_011539527.1:n.2062+21_2062+22insTATAAATAAAGGATTTTGT
XM_011541225.2:c.2062+21_2062+22insTATAAATAAAGGATTTTGT (PTPN22)	XP_011539527.1:n.2062+21_2062+22insTATAAATAAAGGATTTTGT
XM_017001004.1:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22)	XP_016856493.1:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
XM_017001005.2:c.1789+21_1789+22insTATAAATAAAGGATTTTGT (PTPN22)	XP_016856494.1:n.1789+21_1789+22insTATAAATAAAGGATTTTGT
NM_015967.7:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22)	NP_057051.3:n.2134+21_2134+22insTATAAATAAAGGATTTTGT
NM_015967.8:c.2134+21_2134+22insTATAAATAAAGGATTTTGT (PTPN22) MANE Select	NP_057051.4:n.2134+21_2134+22insTATAAATAAAGGATTTTGT