Canonical Allele Identifier: CA1189917120
Gene: PTPN22 HGNC NCBI
AP4B1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1661639538

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113821800_113821801insCAC , CM000663.2:g.113821800_113821801insCAC GRCh38
NC_000001.10:g.114364422_114364423insCAC , CM000663.1:g.114364422_114364423insCAC GRCh37
NC_000001.9:g.114165945_114165946insCAC NCBI36
NG_011432.1:g.54953_54954insGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000359785.10:c.2282-2147_2282-2146insGTG (PTPN22) MANE Select ENSP00000352833.5:n.2282-2147_2282-2146in...
ENST00000359785.9:c.2282-2147_2282-2146insGTG (PTPN22) ENSP00000352833.5:n.2282-2147_2282-2146in...
ENST00000420377.6:c.2282-2147_2282-2146insGTG (PTPN22) ENSP00000388229.2:n.2282-2147_2282-2146in...
ENST00000460620.5:c.469-2147_469-2146insGTG (PTPN22) ENSP00000433141.1:n.469-2147_469-2146insG...
ENST00000525799.1:c.1901-2147_1901-2146insGTG (PTPN22) ENSP00000432674.1:n.1901-2147_1901-2146in...
ENST00000528414.5:c.2117-2147_2117-2146insGTG (PTPN22) ENSP00000435176.1:n.2117-2147_2117-2146in...
ENST00000532224.5:c.*1560-2147_*1560-2146insGTG (PTPN22) ENSP00000431249.1:n.*1560-2147_*1560-2146...
ENST00000538253.5:c.2210-2147_2210-2146insGTG (PTPN22) ENSP00000439372.2:n.2210-2147_2210-2146in...
NM_001193431.1:c.2198-2147_2198-2146insGTG (PTPN22) NP_001180360.1:n.2198-2147_2198-2146insGT...
NM_001193431.2:c.2198-2147_2198-2146insGTG (PTPN22) NP_001180360.1:n.2198-2147_2198-2146insGT...
NM_001308297.1:c.2210-2147_2210-2146insGTG (PTPN22) NP_001295226.1:n.2210-2147_2210-2146insGT...
NM_012411.4:c.2117-2147_2117-2146insGTG (PTPN22) NP_036543.4:n.2117-2147_2117-2146insGTG
NM_012411.5:c.2117-2147_2117-2146insGTG (PTPN22) NP_036543.4:n.2117-2147_2117-2146insGTG
NM_015967.5:c.2282-2147_2282-2146insGTG (PTPN22) NP_057051.3:n.2282-2147_2282-2146insGTG
NM_015967.6:c.2282-2147_2282-2146insGTG (PTPN22) NP_057051.3:n.2282-2147_2282-2146insGTG
NR_125965.1:n.414+6328_414+6329insCAC (AP4B1-AS1)
XM_011541221.1:c.2204-2147_2204-2146insGTG (PTPN22) XP_011539523.1:n.2204-2147_2204-2146insGT...
XM_011541222.1:c.2251-2147_2251-2146insGTG (PTPN22) XP_011539524.1:n.2251-2147_2251-2146insGT...
XM_011541224.1:c.1838-2147_1838-2146insGTG (PTPN22) XP_011539526.1:n.1838-2147_1838-2146insGT...
XM_011541225.1:c.2179-2147_2179-2146insGTG (PTPN22) XP_011539527.1:n.2179-2147_2179-2146insGT...
XM_011541225.2:c.2179-2147_2179-2146insGTG (PTPN22) XP_011539527.1:n.2179-2147_2179-2146insGT...
XM_017001005.2:c.1937-2147_1937-2146insGTG (PTPN22) XP_016856494.1:n.1937-2147_1937-2146insGT...
NM_015967.7:c.2282-2147_2282-2146insGTG (PTPN22) NP_057051.3:n.2282-2147_2282-2146insGTG
NM_015967.8:c.2282-2147_2282-2146insGTG (PTPN22) MANE Select NP_057051.4:n.2282-2147_2282-2146insGTG