Canonical Allele Identifier: CA2530704534

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113863639_113863640insAAG , CM000663.2:g.113863639_113863640insAAG	GRCh38
NC_000001.10:g.114406261_114406262insAAG , CM000663.1:g.114406261_114406262insAAG	GRCh37
NC_000001.9:g.114207784_114207785insAAG	NCBI36
NG_011432.1:g.13114_13115insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.88-4180_88-4179insCTT (PTPN22) MANE Select	ENSP00000352833.5:n.88-4180_88-4179insCTT
ENST00000359785.9:c.88-4180_88-4179insCTT (PTPN22)	ENSP00000352833.5:n.88-4180_88-4179insCTT
ENST00000420377.6:c.88-4180_88-4179insCTT (PTPN22)	ENSP00000388229.2:n.88-4180_88-4179insCTT
ENST00000460620.5:c.88-4180_88-4179insCTT (PTPN22)	ENSP00000433141.1:n.88-4180_88-4179insCTT
ENST00000484147.5:n.129-4180_129-4179insCTT (PTPN22)
ENST00000525799.1:c.88-4180_88-4179insCTT (PTPN22)	ENSP00000432674.1:n.88-4180_88-4179insCTT
ENST00000528414.5:c.88-4180_88-4179insCTT (PTPN22)	ENSP00000435176.1:n.88-4180_88-4179insCTT
ENST00000529045.1:c.272+558_272+559insCTT (PTPN22)	ENSP00000434932.1:n.272+558_272+559insCTT
ENST00000532224.5:c.88-4180_88-4179insCTT (PTPN22)	ENSP00000431249.1:n.88-4180_88-4179insCTT
ENST00000534519.1:n.201-4180_201-4179insCTT (PTPN22)
ENST00000538253.5:c.88-4180_88-4179insCTT (PTPN22)	ENSP00000439372.2:n.88-4180_88-4179insCTT
NM_001193431.1:c.88-4180_88-4179insCTT (PTPN22)	NP_001180360.1:n.88-4180_88-4179insCTT
NM_001193431.2:c.88-4180_88-4179insCTT (PTPN22)	NP_001180360.1:n.88-4180_88-4179insCTT
NM_001308297.1:c.88-4180_88-4179insCTT (PTPN22)	NP_001295226.1:n.88-4180_88-4179insCTT
NM_012411.4:c.88-4180_88-4179insCTT (PTPN22)	NP_036543.4:n.88-4180_88-4179insCTT
NM_012411.5:c.88-4180_88-4179insCTT (PTPN22)	NP_036543.4:n.88-4180_88-4179insCTT
NM_015967.5:c.88-4180_88-4179insCTT (PTPN22)	NP_057051.3:n.88-4180_88-4179insCTT
NM_015967.6:c.88-4180_88-4179insCTT (PTPN22)	NP_057051.3:n.88-4180_88-4179insCTT
NR_037864.1:n.246+5623_246+5624insAAG (AP4B1-AS1)
NR_125965.1:n.415-34229_415-34228insAAG (AP4B1-AS1)
XM_011541221.1:c.88-4180_88-4179insCTT (PTPN22)	XP_011539523.1:n.88-4180_88-4179insCTT
XM_011541222.1:c.88-4180_88-4179insCTT (PTPN22)	XP_011539524.1:n.88-4180_88-4179insCTT
XM_011541223.1:c.88-4180_88-4179insCTT (PTPN22)	XP_011539525.1:n.88-4180_88-4179insCTT
XM_011541224.1:c.-564-4180_-564-4179insCTT (PTPN22)	XP_011539526.1:n.-564-4180_-564-4179insCTT
XM_011541225.1:c.88-4180_88-4179insCTT (PTPN22)	XP_011539527.1:n.88-4180_88-4179insCTT
XM_011541223.2:c.88-4180_88-4179insCTT (PTPN22)	XP_011539525.1:n.88-4180_88-4179insCTT
XM_011541225.2:c.88-4180_88-4179insCTT (PTPN22)	XP_011539527.1:n.88-4180_88-4179insCTT
XM_017001004.1:c.88-4180_88-4179insCTT (PTPN22)	XP_016856493.1:n.88-4180_88-4179insCTT
XM_017001005.2:c.-259+558_-259+559insCTT (PTPN22)	XP_016856494.1:n.-259+558_-259+559insCTT
XM_017001006.1:c.88-4180_88-4179insCTT (PTPN22)	XP_016856495.1:n.88-4180_88-4179insCTT
NM_015967.7:c.88-4180_88-4179insCTT (PTPN22)	NP_057051.3:n.88-4180_88-4179insCTT
NM_015967.8:c.88-4180_88-4179insCTT (PTPN22) MANE Select	NP_057051.4:n.88-4180_88-4179insCTT