Linked Data
dbSNP Id:
rs1447341244
gnomAD v2:
13-48986188-TGAC-T
gnomAD v3:
13-48412052-TGAC-T
gnomAD v4:
13-48412052-TGAC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48412053_48412055del , CM000675.2:g.48412053_48412055del | GRCh38 |
| NC_000013.10:g.48986189_48986191del , CM000675.1:g.48986189_48986191del | GRCh37 |
| NC_000013.9:g.47884190_47884192del | NCBI36 |
| NG_009009.1:g.113307_113309del , LRG_517:g.113307_113309del | |
| NG_012874.1:g.37650_37652del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1695+30610_1695+30612del (RB1) MANE Select | ENSP00000267163.4:n.1695+30610_1695+30612del | |
| ENST00000620633.5:c.369_371del (LPAR6) MANE Select | ENSP00000482660.1:p.Ser124del | |
| ENST00000643064.1:c.194+30610_194+30612del (RB1) | ||
| ENST00000650461.1:c.1695+30610_1695+30612del (RB1) | ENSP00000497193.1:n.1695+30610_1695+30612del | |
| ENST00000267163.4:c.1695+30610_1695+30612del (RB1) | ENSP00000267163.4:n.1695+30610_1695+30612del | |
| ENST00000345941.2:c.369_371del (LPAR6) | ENSP00000344353.2:p.Ser124del | |
| ENST00000378434.8:c.369_371del (LPAR6) | ENSP00000367691.3:p.Ser124del | |
| ENST00000462781.5:n.114+3645_114+3647del (LPAR6) | ||
| ENST00000465365.6:n.1069-3288_1069-3286del (LPAR6) | ||
| ENST00000470937.1:n.117+3645_117+3647del (LPAR6) | ||
| ENST00000482024.1:n.220_222del (LPAR6) | ||
| ENST00000620633.4:c.369_371del (LPAR6) | ENSP00000482660.1:p.Ser124del | |
| NM_000321.2:c.1695+30610_1695+30612del , LRG_517t1:c.1695+30610_1695+30612del (RB1) | NP_000312.2:n.1695+30610_1695+30612del | |
| NM_001162497.1:c.369_371del (LPAR6) | NP_001155969.1:p.Ser124del | |
| NM_001162498.1:c.369_371del (LPAR6) | NP_001155970.1:p.Ser124del | |
| NM_005767.5:c.369_371del (LPAR6) | NP_005758.2:p.Ser124del | |
| XM_011535171.1:c.1434+30610_1434+30612del (RB1) | XP_011533473.1:n.1434+30610_1434+30612del | |
| XM_011535171.2:c.1434+30610_1434+30612del (RB1) | XP_011533473.1:n.1434+30610_1434+30612del | |
| XM_024449302.1:c.369_371del (LPAR6) | XP_024305070.1:p.Ser124del | |
| XM_024449303.1:c.192+3645_192+3647del (LPAR6) | XP_024305071.1:n.192+3645_192+3647del | |
| XM_024449304.1:c.192+3645_192+3647del (LPAR6) | XP_024305072.1:n.192+3645_192+3647del | |
| NM_001162497.2:c.369_371del (LPAR6) | NP_001155969.1:p.Ser124del | |
| NM_001162498.2:c.369_371del (LPAR6) | NP_001155970.1:p.Ser124del | |
| NM_001377316.1:c.369_371del (LPAR6) | NP_001364245.1:p.Ser124del | |
| NM_001377317.1:c.369_371del (LPAR6) | NP_001364246.1:p.Ser124del | |
| NM_005767.6:c.369_371del (LPAR6) | NP_005758.2:p.Ser124del | |
| NM_000321.3:c.1695+30610_1695+30612del (RB1) MANE Select | NP_000312.2:n.1695+30610_1695+30612del | |
| NM_001162497.3:c.369_371del (LPAR6) | NP_001155969.1:p.Ser124del | |
| NM_001162498.3:c.369_371del (LPAR6) MANE Select | NP_001155970.1:p.Ser124del | |
| NM_001377316.2:c.369_371del (LPAR6) | NP_001364245.1:p.Ser124del | |
| NM_001377317.2:c.369_371del (LPAR6) | NP_001364246.1:p.Ser124del | |
| NM_005767.7:c.369_371del (LPAR6) | NP_005758.2:p.Ser124del |