Canonical Allele Identifier: CA1140496634

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113852067C= , CM000663.2:g.113852067C=	GRCh38
NC_000001.10:g.114394689C= , CM000663.1:g.114394689C=	GRCh37
NC_000001.9:g.114196212C=	NCBI36
NG_011432.1:g.24687G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.788G= (PTPN22) MANE Select	ENSP00000352833.5:p.Arg263=
ENST00000359785.9:c.788G= (PTPN22)	ENSP00000352833.5:p.Arg263=
ENST00000420377.6:c.788G= (PTPN22)	ENSP00000388229.2:p.Arg263=
ENST00000460620.5:c.468+4315G= (PTPN22)	ENSP00000433141.1:n.468+4315G=
ENST00000484147.5:n.829G= (PTPN22)
ENST00000525799.1:c.407G= (PTPN22)	ENSP00000432674.1:p.Arg136=
ENST00000528414.5:c.750+2404G= (PTPN22)	ENSP00000435176.1:n.750+2404G=
ENST00000532224.5:c.*66G= (PTPN22)	ENSP00000431249.1:n.*66G=
ENST00000538253.5:c.716G= (PTPN22)	ENSP00000439372.2:p.Arg239=
NM_001193431.1:c.788G= (PTPN22)	NP_001180360.1:p.Arg263=
NM_001193431.2:c.788G= (PTPN22)	NP_001180360.1:p.Arg263=
NM_001308297.1:c.716G= (PTPN22)	NP_001295226.1:p.Arg239=
NM_012411.4:c.750+2404G= (PTPN22)	NP_036543.4:n.750+2404G=
NM_012411.5:c.750+2404G= (PTPN22)	NP_036543.4:n.750+2404G=
NM_015967.5:c.788G= (PTPN22)	NP_057051.3:p.Arg263=
NM_015967.6:c.788G= (PTPN22)	NP_057051.3:p.Arg263=
NR_125965.1:n.414+36595C= (AP4B1-AS1)
XM_011541221.1:c.750+2404G= (PTPN22)	XP_011539523.1:n.750+2404G=
XM_011541222.1:c.788G= (PTPN22)	XP_011539524.1:p.Arg263=
XM_011541223.1:c.788G= (PTPN22)	XP_011539525.1:p.Arg263=
XM_011541224.1:c.344G= (PTPN22)	XP_011539526.1:p.Arg115=
XM_011541225.1:c.716G= (PTPN22)	XP_011539527.1:p.Arg239=
XM_011541223.2:c.788G= (PTPN22)	XP_011539525.1:p.Arg263=
XM_011541225.2:c.716G= (PTPN22)	XP_011539527.1:p.Arg239=
XM_017001004.1:c.788G= (PTPN22)	XP_016856493.1:p.Arg263=
XM_017001005.2:c.443G= (PTPN22)	XP_016856494.1:p.Arg148=
XM_017001006.1:c.788G= (PTPN22)	XP_016856495.1:p.Arg263=
NM_015967.7:c.788G= (PTPN22)	NP_057051.3:p.Arg263=
NM_015967.8:c.788G= (PTPN22) MANE Select	NP_057051.4:p.Arg263=