Canonical Allele Identifier: CA1189916744
Gene: PTPN22 HGNC NCBI
AP4B1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113820853_113820854delinsAG , CM000663.2:g.113820853_113820854delinsAG GRCh38
NC_000001.10:g.114363475_114363476delinsAG , CM000663.1:g.114363475_114363476delinsAG GRCh37
NC_000001.9:g.114164998_114164999delinsAG NCBI36
NG_011432.1:g.55900_55901delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000359785.10:c.2282-1200_2282-1199delinsCT (PTPN22) MANE Select ENSP00000352833.5:n.2282-1200_2282-1199de...
ENST00000359785.9:c.2282-1200_2282-1199delinsCT (PTPN22) ENSP00000352833.5:n.2282-1200_2282-1199de...
ENST00000420377.6:c.2282-1200_2282-1199delinsCT (PTPN22) ENSP00000388229.2:n.2282-1200_2282-1199de...
ENST00000460620.5:c.469-1200_469-1199delinsCT (PTPN22) ENSP00000433141.1:n.469-1200_469-1199deli...
ENST00000525799.1:c.1901-1200_1901-1199delinsCT (PTPN22) ENSP00000432674.1:n.1901-1200_1901-1199de...
ENST00000528414.5:c.2117-1200_2117-1199delinsCT (PTPN22) ENSP00000435176.1:n.2117-1200_2117-1199de...
ENST00000532224.5:c.*1560-1200_*1560-1199delinsCT (PTPN22) ENSP00000431249.1:n.*1560-1200_*1560-1199...
ENST00000538253.5:c.2210-1200_2210-1199delinsCT (PTPN22) ENSP00000439372.2:n.2210-1200_2210-1199de...
NM_001193431.1:c.2198-1200_2198-1199delinsCT (PTPN22) NP_001180360.1:n.2198-1200_2198-1199delin...
NM_001193431.2:c.2198-1200_2198-1199delinsCT (PTPN22) NP_001180360.1:n.2198-1200_2198-1199delin...
NM_001308297.1:c.2210-1200_2210-1199delinsCT (PTPN22) NP_001295226.1:n.2210-1200_2210-1199delin...
NM_012411.4:c.2117-1200_2117-1199delinsCT (PTPN22) NP_036543.4:n.2117-1200_2117-1199delinsCT...
NM_012411.5:c.2117-1200_2117-1199delinsCT (PTPN22) NP_036543.4:n.2117-1200_2117-1199delinsCT...
NM_015967.5:c.2282-1200_2282-1199delinsCT (PTPN22) NP_057051.3:n.2282-1200_2282-1199delinsCT...
NM_015967.6:c.2282-1200_2282-1199delinsCT (PTPN22) NP_057051.3:n.2282-1200_2282-1199delinsCT...
NR_125965.1:n.414+5381_414+5382delinsAG (AP4B1-AS1)
XM_011541221.1:c.2204-1200_2204-1199delinsCT (PTPN22) XP_011539523.1:n.2204-1200_2204-1199delin...
XM_011541222.1:c.2251-1200_2251-1199delinsCT (PTPN22) XP_011539524.1:n.2251-1200_2251-1199delin...
XM_011541224.1:c.1838-1200_1838-1199delinsCT (PTPN22) XP_011539526.1:n.1838-1200_1838-1199delin...
XM_011541225.1:c.2179-1200_2179-1199delinsCT (PTPN22) XP_011539527.1:n.2179-1200_2179-1199delin...
XM_011541225.2:c.2179-1200_2179-1199delinsCT (PTPN22) XP_011539527.1:n.2179-1200_2179-1199delin...
XM_017001005.2:c.1937-1200_1937-1199delinsCT (PTPN22) XP_016856494.1:n.1937-1200_1937-1199delin...
NM_015967.7:c.2282-1200_2282-1199delinsCT (PTPN22) NP_057051.3:n.2282-1200_2282-1199delinsCT...
NM_015967.8:c.2282-1200_2282-1199delinsCT (PTPN22) MANE Select NP_057051.4:n.2282-1200_2282-1199delinsCT...