Canonical Allele Identifier: CA1189920178

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113829806_113829807delinsAT , CM000663.2:g.113829806_113829807delinsAT	GRCh38
NC_000001.10:g.114372428_114372429delinsAT , CM000663.1:g.114372428_114372429delinsAT	GRCh37
NC_000001.9:g.114173951_114173952delinsAT	NCBI36
NG_011432.1:g.46947_46948delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.2135-100_2135-99delinsAT (PTPN22) MANE Select	ENSP00000352833.5:n.2135-100_2135-99delinsAT
ENST00000359785.9:c.2135-100_2135-99delinsAT (PTPN22)	ENSP00000352833.5:n.2135-100_2135-99delinsAT
ENST00000420377.6:c.2135-100_2135-99delinsAT (PTPN22)	ENSP00000388229.2:n.2135-100_2135-99delinsAT
ENST00000460620.5:c.469-10153_469-10152delinsAT (PTPN22)	ENSP00000433141.1:n.469-10153_469-10152delinsAT
ENST00000525799.1:c.1754-100_1754-99delinsAT (PTPN22)	ENSP00000432674.1:n.1754-100_1754-99delinsAT
ENST00000528414.5:c.1970-100_1970-99delinsAT (PTPN22)	ENSP00000435176.1:n.1970-100_1970-99delinsAT
ENST00000532224.5:c.*1413-100_*1413-99delinsAT (PTPN22)	ENSP00000431249.1:n.*1413-100_*1413-99delinsAT
ENST00000538253.5:c.2063-100_2063-99delinsAT (PTPN22)	ENSP00000439372.2:n.2063-100_2063-99delinsAT
NM_001193431.1:c.2051-100_2051-99delinsAT (PTPN22)	NP_001180360.1:n.2051-100_2051-99delinsAT
NM_001193431.2:c.2051-100_2051-99delinsAT (PTPN22)	NP_001180360.1:n.2051-100_2051-99delinsAT
NM_001308297.1:c.2063-100_2063-99delinsAT (PTPN22)	NP_001295226.1:n.2063-100_2063-99delinsAT
NM_012411.4:c.1970-100_1970-99delinsAT (PTPN22)	NP_036543.4:n.1970-100_1970-99delinsAT
NM_012411.5:c.1970-100_1970-99delinsAT (PTPN22)	NP_036543.4:n.1970-100_1970-99delinsAT
NM_015967.5:c.2135-100_2135-99delinsAT (PTPN22)	NP_057051.3:n.2135-100_2135-99delinsAT
NM_015967.6:c.2135-100_2135-99delinsAT (PTPN22)	NP_057051.3:n.2135-100_2135-99delinsAT
NR_125965.1:n.414+14334_414+14335delinsAT (AP4B1-AS1)
XM_011541221.1:c.2057-100_2057-99delinsAT (PTPN22)	XP_011539523.1:n.2057-100_2057-99delinsAT
XM_011541222.1:c.2135-100_2135-99delinsAT (PTPN22)	XP_011539524.1:n.2135-100_2135-99delinsAT
XM_011541224.1:c.1691-100_1691-99delinsAT (PTPN22)	XP_011539526.1:n.1691-100_1691-99delinsAT
XM_011541225.1:c.2063-100_2063-99delinsAT (PTPN22)	XP_011539527.1:n.2063-100_2063-99delinsAT
XM_011541225.2:c.2063-100_2063-99delinsAT (PTPN22)	XP_011539527.1:n.2063-100_2063-99delinsAT
XM_017001004.1:c.2135-100_2135-99delinsAT (PTPN22)	XP_016856493.1:n.2135-100_2135-99delinsAT
XM_017001005.2:c.1790-100_1790-99delinsAT (PTPN22)	XP_016856494.1:n.1790-100_1790-99delinsAT
NM_015967.7:c.2135-100_2135-99delinsAT (PTPN22)	NP_057051.3:n.2135-100_2135-99delinsAT
NM_015967.8:c.2135-100_2135-99delinsAT (PTPN22) MANE Select	NP_057051.4:n.2135-100_2135-99delinsAT