Canonical Allele Identifier: CA1189921990

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113834951G= , CM000663.2:g.113834951G=	GRCh38
NC_000001.10:g.114377573G= , CM000663.1:g.114377573G=	GRCh37
NC_000001.9:g.114179096G=	NCBI36
NG_011432.1:g.41803C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000359785.10:c.1853C= (PTPN22) MANE Select	ENSP00000352833.5:p.Pro618=
ENST00000359785.9:c.1853C= (PTPN22)	ENSP00000352833.5:p.Pro618=
ENST00000420377.6:c.1853C= (PTPN22)	ENSP00000388229.2:p.Pro618=
ENST00000460620.5:c.469-15297C= (PTPN22)	ENSP00000433141.1:n.469-15297C=
ENST00000484147.5:n.1894C= (PTPN22)
ENST00000525799.1:c.1472C= (PTPN22)	ENSP00000432674.1:p.Pro491=
ENST00000528414.5:c.1688C= (PTPN22)	ENSP00000435176.1:p.Pro563=
ENST00000532224.5:c.*1131C= (PTPN22)	ENSP00000431249.1:n.*1131C=
ENST00000538253.5:c.1781C= (PTPN22)	ENSP00000439372.2:p.Pro594=
NM_001193431.1:c.1853C= (PTPN22)	NP_001180360.1:p.Pro618=
NM_001193431.2:c.1853C= (PTPN22)	NP_001180360.1:p.Pro618=
NM_001308297.1:c.1781C= (PTPN22)	NP_001295226.1:p.Pro594=
NM_012411.4:c.1688C= (PTPN22)	NP_036543.4:p.Pro563=
NM_012411.5:c.1688C= (PTPN22)	NP_036543.4:p.Pro563=
NM_015967.5:c.1853C= (PTPN22)	NP_057051.3:p.Pro618=
NM_015967.6:c.1853C= (PTPN22)	NP_057051.3:p.Pro618=
NR_125965.1:n.414+19479G= (AP4B1-AS1)
XM_011541221.1:c.1775C= (PTPN22)	XP_011539523.1:p.Pro592=
XM_011541222.1:c.1853C= (PTPN22)	XP_011539524.1:p.Pro618=
XM_011541223.1:c.1853C= (PTPN22)	XP_011539525.1:p.Pro618=
XM_011541224.1:c.1409C= (PTPN22)	XP_011539526.1:p.Pro470=
XM_011541225.1:c.1781C= (PTPN22)	XP_011539527.1:p.Pro594=
XM_011541223.2:c.1853C= (PTPN22)	XP_011539525.1:p.Pro618=
XM_011541225.2:c.1781C= (PTPN22)	XP_011539527.1:p.Pro594=
XM_017001004.1:c.1853C= (PTPN22)	XP_016856493.1:p.Pro618=
XM_017001005.2:c.1508C= (PTPN22)	XP_016856494.1:p.Pro503=
NM_015967.7:c.1853C= (PTPN22)	NP_057051.3:p.Pro618=
NM_015967.8:c.1853C= (PTPN22) MANE Select	NP_057051.4:p.Pro618=