Canonical Allele Identifier: CA1189921998

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113834974A= , CM000663.2:g.113834974A=	GRCh38
NC_000001.10:g.114377596A= , CM000663.1:g.114377596A=	GRCh37
NC_000001.9:g.114179119A=	NCBI36
NG_011432.1:g.41780T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.1830T= (PTPN22) MANE Select	ENSP00000352833.5:p.Asp610=
ENST00000359785.9:c.1830T= (PTPN22)	ENSP00000352833.5:p.Asp610=
ENST00000420377.6:c.1830T= (PTPN22)	ENSP00000388229.2:p.Asp610=
ENST00000460620.5:c.469-15320T= (PTPN22)	ENSP00000433141.1:n.469-15320T=
ENST00000484147.5:n.1871T= (PTPN22)
ENST00000525799.1:c.1449T= (PTPN22)	ENSP00000432674.1:p.Asp483=
ENST00000528414.5:c.1665T= (PTPN22)	ENSP00000435176.1:p.Asp555=
ENST00000532224.5:c.*1108T= (PTPN22)	ENSP00000431249.1:n.*1108T=
ENST00000538253.5:c.1758T= (PTPN22)	ENSP00000439372.2:p.Asp586=
NM_001193431.1:c.1830T= (PTPN22)	NP_001180360.1:p.Asp610=
NM_001193431.2:c.1830T= (PTPN22)	NP_001180360.1:p.Asp610=
NM_001308297.1:c.1758T= (PTPN22)	NP_001295226.1:p.Asp586=
NM_012411.4:c.1665T= (PTPN22)	NP_036543.4:p.Asp555=
NM_012411.5:c.1665T= (PTPN22)	NP_036543.4:p.Asp555=
NM_015967.5:c.1830T= (PTPN22)	NP_057051.3:p.Asp610=
NM_015967.6:c.1830T= (PTPN22)	NP_057051.3:p.Asp610=
NR_125965.1:n.414+19502A= (AP4B1-AS1)
XM_011541221.1:c.1752T= (PTPN22)	XP_011539523.1:p.Asp584=
XM_011541222.1:c.1830T= (PTPN22)	XP_011539524.1:p.Asp610=
XM_011541223.1:c.1830T= (PTPN22)	XP_011539525.1:p.Asp610=
XM_011541224.1:c.1386T= (PTPN22)	XP_011539526.1:p.Asp462=
XM_011541225.1:c.1758T= (PTPN22)	XP_011539527.1:p.Asp586=
XM_011541223.2:c.1830T= (PTPN22)	XP_011539525.1:p.Asp610=
XM_011541225.2:c.1758T= (PTPN22)	XP_011539527.1:p.Asp586=
XM_017001004.1:c.1830T= (PTPN22)	XP_016856493.1:p.Asp610=
XM_017001005.2:c.1485T= (PTPN22)	XP_016856494.1:p.Asp495=
NM_015967.7:c.1830T= (PTPN22)	NP_057051.3:p.Asp610=
NM_015967.8:c.1830T= (PTPN22) MANE Select	NP_057051.4:p.Asp610=