Canonical Allele Identifier: CA1189921814

Gene: PTPN22 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113834490_113834491delinsCA , CM000663.2:g.113834490_113834491delinsCA	GRCh38
NC_000001.10:g.114377112_114377113delinsCA , CM000663.1:g.114377112_114377113delinsCA	GRCh37
NC_000001.9:g.114178635_114178636delinsCA	NCBI36
NG_011432.1:g.42263_42264delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000359785.10:c.1895-52_1895-51delinsTG (PTPN22) MANE Select	ENSP00000352833.5:n.1895-52_1895-51delinsTG
ENST00000359785.9:c.1895-52_1895-51delinsTG (PTPN22)	ENSP00000352833.5:n.1895-52_1895-51delinsTG
ENST00000420377.6:c.1895-52_1895-51delinsTG (PTPN22)	ENSP00000388229.2:n.1895-52_1895-51delinsTG
ENST00000460620.5:c.469-14837_469-14836delinsTG (PTPN22)	ENSP00000433141.1:n.469-14837_469-14836delinsTG
ENST00000484147.5:n.1936-52_1936-51delinsTG (PTPN22)
ENST00000525799.1:c.1514-52_1514-51delinsTG (PTPN22)	ENSP00000432674.1:n.1514-52_1514-51delinsTG
ENST00000528414.5:c.1730-52_1730-51delinsTG (PTPN22)	ENSP00000435176.1:n.1730-52_1730-51delinsTG
ENST00000532224.5:c.*1173-52_*1173-51delinsTG (PTPN22)	ENSP00000431249.1:n.*1173-52_*1173-51delinsTG
ENST00000538253.5:c.1823-52_1823-51delinsTG (PTPN22)	ENSP00000439372.2:n.1823-52_1823-51delinsTG
NM_001193431.1:c.1895-52_1895-51delinsTG (PTPN22)	NP_001180360.1:n.1895-52_1895-51delinsTG
NM_001193431.2:c.1895-52_1895-51delinsTG (PTPN22)	NP_001180360.1:n.1895-52_1895-51delinsTG
NM_001308297.1:c.1823-52_1823-51delinsTG (PTPN22)	NP_001295226.1:n.1823-52_1823-51delinsTG
NM_012411.4:c.1730-52_1730-51delinsTG (PTPN22)	NP_036543.4:n.1730-52_1730-51delinsTG
NM_012411.5:c.1730-52_1730-51delinsTG (PTPN22)	NP_036543.4:n.1730-52_1730-51delinsTG
NM_015967.5:c.1895-52_1895-51delinsTG (PTPN22)	NP_057051.3:n.1895-52_1895-51delinsTG
NM_015967.6:c.1895-52_1895-51delinsTG (PTPN22)	NP_057051.3:n.1895-52_1895-51delinsTG
NR_125965.1:n.414+19018_414+19019delinsCA (AP4B1-AS1)
XM_011541221.1:c.1817-52_1817-51delinsTG (PTPN22)	XP_011539523.1:n.1817-52_1817-51delinsTG
XM_011541222.1:c.1895-52_1895-51delinsTG (PTPN22)	XP_011539524.1:n.1895-52_1895-51delinsTG
XM_011541223.1:c.1895-52_1895-51delinsTG (PTPN22)	XP_011539525.1:n.1895-52_1895-51delinsTG
XM_011541224.1:c.1451-52_1451-51delinsTG (PTPN22)	XP_011539526.1:n.1451-52_1451-51delinsTG
XM_011541225.1:c.1823-52_1823-51delinsTG (PTPN22)	XP_011539527.1:n.1823-52_1823-51delinsTG
XM_011541223.2:c.1895-52_1895-51delinsTG (PTPN22)	XP_011539525.1:n.1895-52_1895-51delinsTG
XM_011541225.2:c.1823-52_1823-51delinsTG (PTPN22)	XP_011539527.1:n.1823-52_1823-51delinsTG
XM_017001004.1:c.1895-52_1895-51delinsTG (PTPN22)	XP_016856493.1:n.1895-52_1895-51delinsTG
XM_017001005.2:c.1550-52_1550-51delinsTG (PTPN22)	XP_016856494.1:n.1550-52_1550-51delinsTG
NM_015967.7:c.1895-52_1895-51delinsTG (PTPN22)	NP_057051.3:n.1895-52_1895-51delinsTG
NM_015967.8:c.1895-52_1895-51delinsTG (PTPN22) MANE Select	NP_057051.4:n.1895-52_1895-51delinsTG