Linked Data
dbSNP Id:
rs758657737
ExAC:
10:96039598 A / ACCC
gnomAD v2:
10-96039598-A-ACCC
MyVariant Identifiers:
chr10:g.96039598_96039599insCCC (hg19)
chr10:g.94279841_94279842insCCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94279843_94279844insCCC , CM000672.2:g.94279843_94279844insCCC | GRCh38 |
| NC_000010.10:g.96039600_96039601insCCC , CM000672.1:g.96039600_96039601insCCC | GRCh37 |
| NC_000010.9:g.96029590_96029591insCCC | NCBI36 |
| NG_015799.1:g.290855_290856insCCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371375.2:c.3803_3804insCCC (PLCE1) | ENSP00000360426.1:p.Pro1268_Ala1269insPro | |
| ENST00000685253.1:c.*1270_*1271insCCC (PLCE1) | ENSP00000509405.1:n.*1270_*1271insCCC | |
| ENST00000685889.1:n.1462_1463insCCC (PLCE1) | ||
| ENST00000686954.1:c.4727_4728insCCC (PLCE1) | ENSP00000508416.1:p.Pro1576_Ala1577insPro | |
| ENST00000688810.1:c.3755_3756insCCC (PLCE1) | ENSP00000509140.1:p.Pro1252_Ala1253insPro | |
| ENST00000689233.1:n.5057_5058insCCC (PLCE1) | ||
| ENST00000692286.1:c.4727_4728insCCC (PLCE1) | ENSP00000509490.1:p.Pro1576_Ala1577insPro | |
| ENST00000692396.1:c.4679_4680insCCC (PLCE1) | ENSP00000508605.1:p.Pro1560_Ala1561insPro | |
| ENST00000371380.8:c.4727_4728insCCC (PLCE1) MANE Select | ENSP00000360431.2:p.Pro1576_Ala1577insPro | |
| ENST00000371385.8:c.3701_3702insCCC (PLCE1) | ENSP00000360438.4:p.Pro1234_Ala1235insPro | |
| ENST00000674738.1:c.3132_3133insCCC (PLCE1) | ||
| ENST00000674827.1:c.2804_2805insCCC (PLCE1) | ENSP00000502523.1:p.Pro935_Ala936insPro | |
| ENST00000675218.1:c.3803_3804insCCC (PLCE1) | ENSP00000501910.1:p.Pro1268_Ala1269insPro | |
| ENST00000675487.1:c.*660_*661insCCC (PLCE1) | ENSP00000502340.1:n.*660_*661insCCC | |
| ENST00000675718.1:c.3954_3955insCCC (PLCE1) | ||
| ENST00000676102.1:c.3572_3573insCCC (PLCE1) | ENSP00000502811.1:p.Pro1191_Ala1192insPro | |
| ENST00000260766.7:c.4727_4728insCCC (PLCE1) | ENSP00000260766.3:p.Pro1576_Ala1577insPro | |
| ENST00000371375.1:c.3803_3804insCCC (PLCE1) | ENSP00000360426.1:p.Pro1268_Ala1269insPro | |
| ENST00000371380.7:c.4727_4728insCCC (PLCE1) | ENSP00000360431.2:p.Pro1576_Ala1577insPro | |
| ENST00000371385.7:c.3803_3804insCCC (PLCE1) | ENSP00000360438.3:p.Pro1268_Ala1269insPro | |
| NM_001165979.2:c.3803_3804insCCC (PLCE1) | NP_001159451.1:p.Pro1268_Ala1269insPro | |
| NM_001288989.1:c.4679_4680insCCC (PLCE1) | NP_001275918.1:p.Pro1560_Ala1561insPro | |
| NM_016341.3:c.4727_4728insCCC (PLCE1) | NP_057425.3:p.Pro1576_Ala1577insPro | |
| NR_033969.1:n.856_857insGGG (PLCE1-AS1) | ||
| XM_006717885.2:c.4727_4728insCCC (PLCE1) | XP_006717948.1:p.Pro1576_Ala1577insPro | |
| XM_006717886.2:c.4727_4728insCCC (PLCE1) | XP_006717949.1:p.Pro1576_Ala1577insPro | |
| XM_006717888.2:c.4727_4728insCCC (PLCE1) | XP_006717951.1:p.Pro1576_Ala1577insPro | |
| XM_006717889.2:c.4679_4680insCCC (PLCE1) | XP_006717952.1:p.Pro1560_Ala1561insPro | |
| XM_006717890.1:c.3803_3804insCCC (PLCE1) | XP_006717953.1:p.Pro1268_Ala1269insPro | |
| XM_011539849.1:c.4727_4728insCCC (PLCE1) | XP_011538151.1:p.Pro1576_Ala1577insPro | |
| XM_011539850.1:c.3572_3573insCCC (PLCE1) | XP_011538152.1:p.Pro1191_Ala1192insPro | |
| XM_011539851.1:c.4727_4728insCCC (PLCE1) | XP_011538153.1:p.Pro1576_Ala1577insPro | |
| XM_011539852.1:c.4727_4728insCCC (PLCE1) | XP_011538154.1:p.Pro1576_Ala1577insPro | |
| XM_006717885.4:c.4727_4728insCCC (PLCE1) | XP_006717948.1:p.Pro1576_Ala1577insPro | |
| XM_006717888.4:c.4727_4728insCCC (PLCE1) | XP_006717951.1:p.Pro1576_Ala1577insPro | |
| XM_006717889.4:c.4679_4680insCCC (PLCE1) | XP_006717952.1:p.Pro1560_Ala1561insPro | |
| XM_006717890.3:c.3803_3804insCCC (PLCE1) | XP_006717953.1:p.Pro1268_Ala1269insPro | |
| XM_011539849.3:c.4727_4728insCCC (PLCE1) | XP_011538151.1:p.Pro1576_Ala1577insPro | |
| XM_011539850.3:c.3572_3573insCCC (PLCE1) | XP_011538152.1:p.Pro1191_Ala1192insPro | |
| XM_011539851.3:c.4727_4728insCCC (PLCE1) | XP_011538153.1:p.Pro1576_Ala1577insPro | |
| XM_011539852.3:c.4727_4728insCCC (PLCE1) | XP_011538154.1:p.Pro1576_Ala1577insPro | |
| XM_017016310.2:c.4727_4728insCCC (PLCE1) | XP_016871799.1:p.Pro1576_Ala1577insPro | |
| XM_017016311.2:c.4727_4728insCCC (PLCE1) | XP_016871800.1:p.Pro1576_Ala1577insPro | |
| XM_017016312.2:c.3755_3756insCCC (PLCE1) | XP_016871801.1:p.Pro1252_Ala1253insPro | |
| NM_001288989.2:c.4679_4680insCCC (PLCE1) | NP_001275918.1:p.Pro1560_Ala1561insPro | |
| NM_016341.4:c.4727_4728insCCC (PLCE1) MANE Select | NP_057425.3:p.Pro1576_Ala1577insPro |