Canonical Allele Identifier: CA1189917097

Gene: PTPN22 AP4B1-AS1

Linked Data

• dbSNP Id: rs1661633912

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113821751_113821752insTTA , CM000663.2:g.113821751_113821752insTTA	GRCh38
NC_000001.10:g.114364373_114364374insTTA , CM000663.1:g.114364373_114364374insTTA	GRCh37
NC_000001.9:g.114165896_114165897insTTA	NCBI36
NG_011432.1:g.55002_55003insTAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000359785.10:c.2282-2098_2282-2097insTAA (PTPN22) MANE Select	ENSP00000352833.5:n.2282-2098_2282-2097in...
ENST00000359785.9:c.2282-2098_2282-2097insTAA (PTPN22)	ENSP00000352833.5:n.2282-2098_2282-2097in...
ENST00000420377.6:c.2282-2098_2282-2097insTAA (PTPN22)	ENSP00000388229.2:n.2282-2098_2282-2097in...
ENST00000460620.5:c.469-2098_469-2097insTAA (PTPN22)	ENSP00000433141.1:n.469-2098_469-2097insT...
ENST00000525799.1:c.1901-2098_1901-2097insTAA (PTPN22)	ENSP00000432674.1:n.1901-2098_1901-2097in...
ENST00000528414.5:c.2117-2098_2117-2097insTAA (PTPN22)	ENSP00000435176.1:n.2117-2098_2117-2097in...
ENST00000532224.5:c.*1560-2098_*1560-2097insTAA (PTPN22)	ENSP00000431249.1:n.*1560-2098_*1560-2097...
ENST00000538253.5:c.2210-2098_2210-2097insTAA (PTPN22)	ENSP00000439372.2:n.2210-2098_2210-2097in...
NM_001193431.1:c.2198-2098_2198-2097insTAA (PTPN22)	NP_001180360.1:n.2198-2098_2198-2097insTA...
NM_001193431.2:c.2198-2098_2198-2097insTAA (PTPN22)	NP_001180360.1:n.2198-2098_2198-2097insTA...
NM_001308297.1:c.2210-2098_2210-2097insTAA (PTPN22)	NP_001295226.1:n.2210-2098_2210-2097insTA...
NM_012411.4:c.2117-2098_2117-2097insTAA (PTPN22)	NP_036543.4:n.2117-2098_2117-2097insTAA
NM_012411.5:c.2117-2098_2117-2097insTAA (PTPN22)	NP_036543.4:n.2117-2098_2117-2097insTAA
NM_015967.5:c.2282-2098_2282-2097insTAA (PTPN22)	NP_057051.3:n.2282-2098_2282-2097insTAA
NM_015967.6:c.2282-2098_2282-2097insTAA (PTPN22)	NP_057051.3:n.2282-2098_2282-2097insTAA
NR_125965.1:n.414+6279_414+6280insTTA (AP4B1-AS1)
XM_011541221.1:c.2204-2098_2204-2097insTAA (PTPN22)	XP_011539523.1:n.2204-2098_2204-2097insTA...
XM_011541222.1:c.2251-2098_2251-2097insTAA (PTPN22)	XP_011539524.1:n.2251-2098_2251-2097insTA...
XM_011541224.1:c.1838-2098_1838-2097insTAA (PTPN22)	XP_011539526.1:n.1838-2098_1838-2097insTA...
XM_011541225.1:c.2179-2098_2179-2097insTAA (PTPN22)	XP_011539527.1:n.2179-2098_2179-2097insTA...
XM_011541225.2:c.2179-2098_2179-2097insTAA (PTPN22)	XP_011539527.1:n.2179-2098_2179-2097insTA...
XM_017001005.2:c.1937-2098_1937-2097insTAA (PTPN22)	XP_016856494.1:n.1937-2098_1937-2097insTA...
NM_015967.7:c.2282-2098_2282-2097insTAA (PTPN22)	NP_057051.3:n.2282-2098_2282-2097insTAA
NM_015967.8:c.2282-2098_2282-2097insTAA (PTPN22) MANE Select	NP_057051.4:n.2282-2098_2282-2097insTAA