Canonical Allele Identifier: CA10906949
Gene: PTPN22 HGNC NCBI
AP4B1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2243471

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113863380G>A , CM000663.2:g.113863380G>A GRCh38
NC_000001.10:g.114406002G>A , CM000663.1:g.114406002G>A GRCh37
NC_000001.9:g.114207525G>A NCBI36
NG_011432.1:g.13374C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359785.10:c.88-3920C>T ENSP00000352833.5:p.=
ENST00000359785.9:c.88-3920C>T ENSP00000352833.5:p.=
ENST00000420377.6:c.88-3920C>T ENSP00000388229.2:p.=
ENST00000460620.5:c.88-3920C>T ENSP00000433141.1:p.=
ENST00000484147.5:n.129-3920C>T
ENST00000525799.1:c.88-3920C>T ENSP00000432674.1:p.=
ENST00000528414.5:c.88-3920C>T ENSP00000435176.1:p.=
ENST00000529045.1:c.272+818C>T ENSP00000434932.1:p.=
ENST00000532224.5:c.88-3920C>T ENSP00000431249.1:p.=
ENST00000534519.1:n.201-3920C>T
ENST00000538253.5:c.88-3920C>T ENSP00000439372.2:p.=
NM_001193431.1:c.88-3920C>T (PTPN22) NP_001180360.1:p.=
NM_001193431.2:c.88-3920C>T (PTPN22) NP_001180360.1:p.=
NM_001308297.1:c.88-3920C>T (PTPN22) NP_001295226.1:p.=
NM_012411.4:c.88-3920C>T (PTPN22) NP_036543.4:p.=
NM_012411.5:c.88-3920C>T (PTPN22) NP_036543.4:p.=
NM_015967.5:c.88-3920C>T (PTPN22) NP_057051.3:p.=
NM_015967.6:c.88-3920C>T (PTPN22) NP_057051.3:p.=
NR_037864.1:n.246+5364G>A (AP4B1-AS1)
NR_125965.1:n.415-34488G>A (AP4B1-AS1)
XM_011541221.1:c.88-3920C>T (PTPN22) XP_011539523.1:p.=
XM_011541222.1:c.88-3920C>T (PTPN22) XP_011539524.1:p.=
XM_011541223.1:c.88-3920C>T (PTPN22) XP_011539525.1:p.=
XM_011541224.1:c.-564-3920C>T (PTPN22) XP_011539526.1:p.=
XM_011541225.1:c.88-3920C>T (PTPN22) XP_011539527.1:p.=
XM_011541223.2:c.88-3920C>T (PTPN22) XP_011539525.1:p.=
XM_011541225.2:c.88-3920C>T (PTPN22) XP_011539527.1:p.=
XM_017001004.1:c.88-3920C>T (PTPN22) XP_016856493.1:p.=
XM_017001005.2:c.-259+818C>T (PTPN22) XP_016856494.1:p.=
XM_017001006.1:c.88-3920C>T (PTPN22) XP_016856495.1:p.=
NM_015967.7:c.88-3920C>T (PTPN22) NP_057051.3:p.=