Canonical Allele Identifier: CA1189926699

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113847020_113847022delinsTAG , CM000663.2:g.113847020_113847022delinsTAG	GRCh38
NC_000001.10:g.114389642_114389644delinsTAG , CM000663.1:g.114389642_114389644delinsTAG	GRCh37
NC_000001.9:g.114191165_114191167delinsTAG	NCBI36
NG_011432.1:g.29732_29734delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.915+1518_915+1520delinsCTA (PTPN22) MANE Select	ENSP00000352833.5:n.915+1518_915+1520delinsCTA
ENST00000359785.9:c.915+1518_915+1520delinsCTA (PTPN22)	ENSP00000352833.5:n.915+1518_915+1520delinsCTA
ENST00000420377.6:c.915+1518_915+1520delinsCTA (PTPN22)	ENSP00000388229.2:n.915+1518_915+1520delinsCTA
ENST00000460620.5:c.468+9360_468+9362delinsCTA (PTPN22)	ENSP00000433141.1:n.468+9360_468+9362delinsCTA
ENST00000484147.5:n.956+1518_956+1520delinsCTA (PTPN22)
ENST00000525799.1:c.534+1518_534+1520delinsCTA (PTPN22)	ENSP00000432674.1:n.534+1518_534+1520delinsCTA
ENST00000528414.5:c.750+7449_750+7451delinsCTA (PTPN22)	ENSP00000435176.1:n.750+7449_750+7451delinsCTA
ENST00000532224.5:c.*193+1518_*193+1520delinsCTA (PTPN22)	ENSP00000431249.1:n.*193+1518_*193+1520delinsCTA
ENST00000538253.5:c.843+1518_843+1520delinsCTA (PTPN22)	ENSP00000439372.2:n.843+1518_843+1520delinsCTA
NM_001193431.1:c.915+1518_915+1520delinsCTA (PTPN22)	NP_001180360.1:n.915+1518_915+1520delinsCTA
NM_001193431.2:c.915+1518_915+1520delinsCTA (PTPN22)	NP_001180360.1:n.915+1518_915+1520delinsCTA
NM_001308297.1:c.843+1518_843+1520delinsCTA (PTPN22)	NP_001295226.1:n.843+1518_843+1520delinsCTA
NM_012411.4:c.750+7449_750+7451delinsCTA (PTPN22)	NP_036543.4:n.750+7449_750+7451delinsCTA
NM_012411.5:c.750+7449_750+7451delinsCTA (PTPN22)	NP_036543.4:n.750+7449_750+7451delinsCTA
NM_015967.5:c.915+1518_915+1520delinsCTA (PTPN22)	NP_057051.3:n.915+1518_915+1520delinsCTA
NM_015967.6:c.915+1518_915+1520delinsCTA (PTPN22)	NP_057051.3:n.915+1518_915+1520delinsCTA
NR_125965.1:n.414+31548_414+31550delinsTAG (AP4B1-AS1)
XM_011541221.1:c.837+1518_837+1520delinsCTA (PTPN22)	XP_011539523.1:n.837+1518_837+1520delinsCTA
XM_011541222.1:c.915+1518_915+1520delinsCTA (PTPN22)	XP_011539524.1:n.915+1518_915+1520delinsCTA
XM_011541223.1:c.915+1518_915+1520delinsCTA (PTPN22)	XP_011539525.1:n.915+1518_915+1520delinsCTA
XM_011541224.1:c.471+1518_471+1520delinsCTA (PTPN22)	XP_011539526.1:n.471+1518_471+1520delinsCTA
XM_011541225.1:c.843+1518_843+1520delinsCTA (PTPN22)	XP_011539527.1:n.843+1518_843+1520delinsCTA
XM_011541223.2:c.915+1518_915+1520delinsCTA (PTPN22)	XP_011539525.1:n.915+1518_915+1520delinsCTA
XM_011541225.2:c.843+1518_843+1520delinsCTA (PTPN22)	XP_011539527.1:n.843+1518_843+1520delinsCTA
XM_017001004.1:c.915+1518_915+1520delinsCTA (PTPN22)	XP_016856493.1:n.915+1518_915+1520delinsCTA
XM_017001005.2:c.570+1518_570+1520delinsCTA (PTPN22)	XP_016856494.1:n.570+1518_570+1520delinsCTA
XM_017001006.1:c.915+1518_915+1520delinsCTA (PTPN22)	XP_016856495.1:n.915+1518_915+1520delinsCTA
NM_015967.7:c.915+1518_915+1520delinsCTA (PTPN22)	NP_057051.3:n.915+1518_915+1520delinsCTA
NM_015967.8:c.915+1518_915+1520delinsCTA (PTPN22) MANE Select	NP_057051.4:n.915+1518_915+1520delinsCTA