Linked Data
dbSNP Id:
rs1217414
gnomAD v2:
1-114412667-G-A
gnomAD v3:
1-113870045-G-A
gnomAD v4:
1-113870045-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.113870045G>A , CM000663.2:g.113870045G>A | GRCh38 |
| NC_000001.10:g.114412667G>A , CM000663.1:g.114412667G>A | GRCh37 |
| NC_000001.9:g.114214190G>A | NCBI36 |
| NG_011432.1:g.6709C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359785.10:c.87+1492C>T (PTPN22) MANE Select | ENSP00000352833.5:n.87+1492C>T | |
| ENST00000359785.9:c.87+1492C>T (PTPN22) | ENSP00000352833.5:n.87+1492C>T | |
| ENST00000420377.6:c.87+1492C>T (PTPN22) | ENSP00000388229.2:n.87+1492C>T | |
| ENST00000460620.5:c.87+1492C>T (PTPN22) | ENSP00000433141.1:n.87+1492C>T | |
| ENST00000484147.5:n.128+1492C>T (PTPN22) | ||
| ENST00000525799.1:c.87+1492C>T (PTPN22) | ENSP00000432674.1:n.87+1492C>T | |
| ENST00000528414.5:c.87+1492C>T (PTPN22) | ENSP00000435176.1:n.87+1492C>T | |
| ENST00000529045.1:c.87+1492C>T (PTPN22) | ENSP00000434932.1:n.87+1492C>T | |
| ENST00000532224.5:c.87+1492C>T (PTPN22) | ENSP00000431249.1:n.87+1492C>T | |
| ENST00000534519.1:n.200+1492C>T (PTPN22) | ||
| ENST00000538253.5:c.87+1492C>T (PTPN22) | ENSP00000439372.2:n.87+1492C>T | |
| NM_001193431.1:c.87+1492C>T (PTPN22) | NP_001180360.1:n.87+1492C>T | |
| NM_001193431.2:c.87+1492C>T (PTPN22) | NP_001180360.1:n.87+1492C>T | |
| NM_001308297.1:c.87+1492C>T (PTPN22) | NP_001295226.1:n.87+1492C>T | |
| NM_012411.4:c.87+1492C>T (PTPN22) | NP_036543.4:n.87+1492C>T | |
| NM_012411.5:c.87+1492C>T (PTPN22) | NP_036543.4:n.87+1492C>T | |
| NM_015967.5:c.87+1492C>T (PTPN22) | NP_057051.3:n.87+1492C>T | |
| NM_015967.6:c.87+1492C>T (PTPN22) | NP_057051.3:n.87+1492C>T | |
| NR_037864.1:n.246+12029G>A (AP4B1-AS1) | ||
| NR_125965.1:n.415-27823G>A (AP4B1-AS1) | ||
| XM_011541221.1:c.87+1492C>T (PTPN22) | XP_011539523.1:n.87+1492C>T | |
| XM_011541222.1:c.87+1492C>T (PTPN22) | XP_011539524.1:n.87+1492C>T | |
| XM_011541223.1:c.87+1492C>T (PTPN22) | XP_011539525.1:n.87+1492C>T | |
| XM_011541224.1:c.-565+1492C>T (PTPN22) | XP_011539526.1:n.-565+1492C>T | |
| XM_011541225.1:c.87+1492C>T (PTPN22) | XP_011539527.1:n.87+1492C>T | |
| XM_011541223.2:c.87+1492C>T (PTPN22) | XP_011539525.1:n.87+1492C>T | |
| XM_011541225.2:c.87+1492C>T (PTPN22) | XP_011539527.1:n.87+1492C>T | |
| XM_017001004.1:c.87+1492C>T (PTPN22) | XP_016856493.1:n.87+1492C>T | |
| XM_017001006.1:c.87+1492C>T (PTPN22) | XP_016856495.1:n.87+1492C>T | |
| NM_015967.7:c.87+1492C>T (PTPN22) | NP_057051.3:n.87+1492C>T | |
| NM_015967.8:c.87+1492C>T (PTPN22) MANE Select | NP_057051.4:n.87+1492C>T |