Canonical Allele Identifier: CA1189923677

Gene: PTPN22 AP4B1-AS1

Linked Data

• dbSNP Id: rs1663319215

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113839409A>G , CM000663.2:g.113839409A>G	GRCh38
NC_000001.10:g.114382031A>G , CM000663.1:g.114382031A>G	GRCh37
NC_000001.9:g.114183554A>G	NCBI36
NG_011432.1:g.37345T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359785.10:c.916-789T>C (PTPN22) MANE Select	ENSP00000352833.5:n.916-789T>C
ENST00000359785.9:c.916-789T>C (PTPN22)	ENSP00000352833.5:n.916-789T>C
ENST00000420377.6:c.916-789T>C (PTPN22)	ENSP00000388229.2:n.916-789T>C
ENST00000460620.5:c.468+16973T>C (PTPN22)	ENSP00000433141.1:n.468+16973T>C
ENST00000484147.5:n.957-789T>C (PTPN22)
ENST00000525799.1:c.535-789T>C (PTPN22)	ENSP00000432674.1:n.535-789T>C
ENST00000528414.5:c.751-789T>C (PTPN22)	ENSP00000435176.1:n.751-789T>C
ENST00000532224.5:c.*194-789T>C (PTPN22)	ENSP00000431249.1:n.*194-789T>C
ENST00000538253.5:c.844-789T>C (PTPN22)	ENSP00000439372.2:n.844-789T>C
NM_001193431.1:c.916-789T>C (PTPN22)	NP_001180360.1:n.916-789T>C
NM_001193431.2:c.916-789T>C (PTPN22)	NP_001180360.1:n.916-789T>C
NM_001308297.1:c.844-789T>C (PTPN22)	NP_001295226.1:n.844-789T>C
NM_012411.4:c.751-789T>C (PTPN22)	NP_036543.4:n.751-789T>C
NM_012411.5:c.751-789T>C (PTPN22)	NP_036543.4:n.751-789T>C
NM_015967.5:c.916-789T>C (PTPN22)	NP_057051.3:n.916-789T>C
NM_015967.6:c.916-789T>C (PTPN22)	NP_057051.3:n.916-789T>C
NR_125965.1:n.414+23937A>G (AP4B1-AS1)
XM_011541221.1:c.838-789T>C (PTPN22)	XP_011539523.1:n.838-789T>C
XM_011541222.1:c.916-789T>C (PTPN22)	XP_011539524.1:n.916-789T>C
XM_011541223.1:c.916-789T>C (PTPN22)	XP_011539525.1:n.916-789T>C
XM_011541224.1:c.472-789T>C (PTPN22)	XP_011539526.1:n.472-789T>C
XM_011541225.1:c.844-789T>C (PTPN22)	XP_011539527.1:n.844-789T>C
XM_011541223.2:c.916-789T>C (PTPN22)	XP_011539525.1:n.916-789T>C
XM_011541225.2:c.844-789T>C (PTPN22)	XP_011539527.1:n.844-789T>C
XM_017001004.1:c.916-789T>C (PTPN22)	XP_016856493.1:n.916-789T>C
XM_017001005.2:c.571-789T>C (PTPN22)	XP_016856494.1:n.571-789T>C
XM_017001006.1:c.916-766T>C (PTPN22)	XP_016856495.1:n.916-766T>C
NM_015967.7:c.916-789T>C (PTPN22)	NP_057051.3:n.916-789T>C
NM_015967.8:c.916-789T>C (PTPN22) MANE Select	NP_057051.4:n.916-789T>C