Canonical Allele Identifier: CA1189920192

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113829837G= , CM000663.2:g.113829837G=	GRCh38
NC_000001.10:g.114372459G= , CM000663.1:g.114372459G=	GRCh37
NC_000001.9:g.114173982G=	NCBI36
NG_011432.1:g.46917C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.2134+112C= (PTPN22) MANE Select	ENSP00000352833.5:n.2134+112C=
ENST00000359785.9:c.2134+112C= (PTPN22)	ENSP00000352833.5:n.2134+112C=
ENST00000420377.6:c.2134+112C= (PTPN22)	ENSP00000388229.2:n.2134+112C=
ENST00000460620.5:c.469-10183C= (PTPN22)	ENSP00000433141.1:n.469-10183C=
ENST00000525799.1:c.1753+112C= (PTPN22)	ENSP00000432674.1:n.1753+112C=
ENST00000528414.5:c.1969+112C= (PTPN22)	ENSP00000435176.1:n.1969+112C=
ENST00000532224.5:c.*1412+112C= (PTPN22)	ENSP00000431249.1:n.*1412+112C=
ENST00000538253.5:c.2062+112C= (PTPN22)	ENSP00000439372.2:n.2062+112C=
NM_001193431.1:c.2050+112C= (PTPN22)	NP_001180360.1:n.2050+112C=
NM_001193431.2:c.2050+112C= (PTPN22)	NP_001180360.1:n.2050+112C=
NM_001308297.1:c.2062+112C= (PTPN22)	NP_001295226.1:n.2062+112C=
NM_012411.4:c.1969+112C= (PTPN22)	NP_036543.4:n.1969+112C=
NM_012411.5:c.1969+112C= (PTPN22)	NP_036543.4:n.1969+112C=
NM_015967.5:c.2134+112C= (PTPN22)	NP_057051.3:n.2134+112C=
NM_015967.6:c.2134+112C= (PTPN22)	NP_057051.3:n.2134+112C=
NR_125965.1:n.414+14365G= (AP4B1-AS1)
XM_011541221.1:c.2056+112C= (PTPN22)	XP_011539523.1:n.2056+112C=
XM_011541222.1:c.2134+112C= (PTPN22)	XP_011539524.1:n.2134+112C=
XM_011541224.1:c.1690+112C= (PTPN22)	XP_011539526.1:n.1690+112C=
XM_011541225.1:c.2062+112C= (PTPN22)	XP_011539527.1:n.2062+112C=
XM_011541225.2:c.2062+112C= (PTPN22)	XP_011539527.1:n.2062+112C=
XM_017001004.1:c.2134+112C= (PTPN22)	XP_016856493.1:n.2134+112C=
XM_017001005.2:c.1789+112C= (PTPN22)	XP_016856494.1:n.1789+112C=
NM_015967.7:c.2134+112C= (PTPN22)	NP_057051.3:n.2134+112C=
NM_015967.8:c.2134+112C= (PTPN22) MANE Select	NP_057051.4:n.2134+112C=