Canonical Allele Identifier: CA419561546

Gene: PTPN22 AP4B1-AS1

Linked Data

• dbSNP Id: rs1662857595
• gnomAD v4: 1-113834965-G-A
• MyVariant Identifiers: chr1:g.114377587G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113834965G>A , CM000663.2:g.113834965G>A	GRCh38
NC_000001.10:g.114377587G>A , CM000663.1:g.114377587G>A	GRCh37
NC_000001.9:g.114179110G>A	NCBI36
NG_011432.1:g.41789C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359785.10:c.1839C>T (PTPN22) MANE Select	ENSP00000352833.5:p.Ile613=
ENST00000359785.9:c.1839C>T (PTPN22)	ENSP00000352833.5:p.Ile613=
ENST00000420377.6:c.1839C>T (PTPN22)	ENSP00000388229.2:p.Ile613=
ENST00000460620.5:c.469-15311C>T (PTPN22)	ENSP00000433141.1:n.469-15311C>T
ENST00000484147.5:n.1880C>T (PTPN22)
ENST00000525799.1:c.1458C>T (PTPN22)	ENSP00000432674.1:p.Ile486=
ENST00000528414.5:c.1674C>T (PTPN22)	ENSP00000435176.1:p.Ile558=
ENST00000532224.5:c.*1117C>T (PTPN22)	ENSP00000431249.1:n.*1117C>T
ENST00000538253.5:c.1767C>T (PTPN22)	ENSP00000439372.2:p.Ile589=
NM_001193431.1:c.1839C>T (PTPN22)	NP_001180360.1:p.Ile613=
NM_001193431.2:c.1839C>T (PTPN22)	NP_001180360.1:p.Ile613=
NM_001308297.1:c.1767C>T (PTPN22)	NP_001295226.1:p.Ile589=
NM_012411.4:c.1674C>T (PTPN22)	NP_036543.4:p.Ile558=
NM_012411.5:c.1674C>T (PTPN22)	NP_036543.4:p.Ile558=
NM_015967.5:c.1839C>T (PTPN22)	NP_057051.3:p.Ile613=
NM_015967.6:c.1839C>T (PTPN22)	NP_057051.3:p.Ile613=
NR_125965.1:n.414+19493G>A (AP4B1-AS1)
XM_011541221.1:c.1761C>T (PTPN22)	XP_011539523.1:p.Ile587=
XM_011541222.1:c.1839C>T (PTPN22)	XP_011539524.1:p.Ile613=
XM_011541223.1:c.1839C>T (PTPN22)	XP_011539525.1:p.Ile613=
XM_011541224.1:c.1395C>T (PTPN22)	XP_011539526.1:p.Ile465=
XM_011541225.1:c.1767C>T (PTPN22)	XP_011539527.1:p.Ile589=
XM_011541223.2:c.1839C>T (PTPN22)	XP_011539525.1:p.Ile613=
XM_011541225.2:c.1767C>T (PTPN22)	XP_011539527.1:p.Ile589=
XM_017001004.1:c.1839C>T (PTPN22)	XP_016856493.1:p.Ile613=
XM_017001005.2:c.1494C>T (PTPN22)	XP_016856494.1:p.Ile498=
NM_015967.7:c.1839C>T (PTPN22)	NP_057051.3:p.Ile613=
NM_015967.8:c.1839C>T (PTPN22) MANE Select	NP_057051.4:p.Ile613=