Linked Data
ClinVar Variation Id:
89800
ClinVar RCV Id:
RCV000075274
dbSNP Id:
rs63751891
PubMed:
PMID:17453009
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.36993562_36993575del , CM000665.2:g.36993562_36993575del | GRCh38 |
| NC_000003.11:g.37035053_37035066del , CM000665.1:g.37035053_37035066del | GRCh37 |
| NC_000003.10:g.37010057_37010070del | NCBI36 |
| NG_007109.2:g.5213_5226del , LRG_216:g.5213_5226del | |
| NG_008418.1:g.4733_4746del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000413740.2:c.15_28del | ENSP00000416476.2:p.Gly6AlafsTer20 | |
| ENST00000450420.6:c.15_28del | ENSP00000393006.2:p.Gly6AlafsTer20 | |
| ENST00000456676.7:c.15_28del | ENSP00000416687.3:p.Gly6AlafsTer20 | |
| ENST00000458009.6:c.15_28del | ENSP00000411066.2:p.Gly6AlafsTer20 | |
| ENST00000616768.6:c.15_28del | ENSP00000480669.3:p.Gly6AlafsTer20 | |
| ENST00000673673.2:c.15_28del | ENSP00000500979.2:p.Gly6AlafsTer20 | |
| ENST00000231790.8:c.15_28del MANE Select | ENSP00000231790.3:p.Gly6AlafsTer20 | |
| ENST00000432299.6:c.15_28del | ENSP00000416783.1:p.Gly6AlafsTer20 | |
| ENST00000442249.6:n.30_43del | ||
| ENST00000673713.1:n.46_59del | ||
| ENST00000673715.1:c.15_28del | ENSP00000501301.1:p.Gly6AlafsTer20 | |
| ENST00000673897.1:c.15_28del | ENSP00000501109.1:p.Gly6AlafsTer20 | |
| ENST00000673899.1:c.15_28del | ENSP00000501030.1:p.Gly6AlafsTer20 | |
| ENST00000673947.1:c.15_28del | ENSP00000501304.1:p.Gly6AlafsTer20 | |
| ENST00000673972.1:c.15_28del | ENSP00000501281.1:p.Gly6AlafsTer20 | |
| ENST00000674111.1:c.15_28del | ENSP00000501162.1:p.Gly6AlafsTer20 | |
| ENST00000231790.6:c.15_28del | ENSP00000231790.2:p.Gly6AlafsTer20 | |
| ENST00000432299.5:c.15_28del | ENSP00000416783.1:p.Gly6AlafsTer20 | |
| ENST00000442249.5:c.15_28del | ENSP00000387511.1:p.Gly6AlafsTer20 | |
| ENST00000454028.5:c.15_28del | ENSP00000392649.1:p.Gly6AlafsTer20 | |
| ENST00000457004.5:c.15_28del | ENSP00000407773.1:p.Gly6AlafsTer20 | |
| ENST00000536378.5:c.-618_-605del | ENSP00000444286.2:n.-618_-605del | |
| NM_000249.3:c.15_28del , LRG_216t1:c.15_28del | NP_000240.1:p.Gly6AlafsTer20 | |
| NM_001258271.1:c.15_28del | NP_001245200.1:p.Gly6AlafsTer20 | |
| NM_001258273.1:c.-618_-605del | NP_001245202.1:n.-618_-605del | |
| XM_005265161.1:c.15_28del | XP_005265218.1:p.Gly6AlafsTer20 | |
| XM_005265164.1:c.-704_-691del | XP_005265221.1:n.-704_-691del | |
| NM_001167617.2:c.-502_-489del | NP_001161089.1:n.-502_-489del | |
| NM_001167618.2:c.-931_-918del | NP_001161090.1:n.-931_-918del | |
| NM_001167619.2:c.-844_-831del | NP_001161091.1:n.-844_-831del | |
| NM_001258274.2:c.-1081_-1068del | NP_001245203.1:n.-1081_-1068del | |
| NM_001354615.1:c.-612_-599del | NP_001341544.1:n.-612_-599del | |
| NM_001354616.1:c.-612_-599del | NP_001341545.1:n.-612_-599del | |
| NM_001354617.1:c.-704_-691del | NP_001341546.1:n.-704_-691del | |
| NM_001354618.1:c.-936_-923del | NP_001341547.1:n.-936_-923del | |
| NM_001354619.1:c.-1060_-1047del | NP_001341548.1:n.-1060_-1047del | |
| NM_001354620.1:c.-270_-257del | NP_001341549.1:n.-270_-257del | |
| NM_001354621.1:c.-1029_-1016del | NP_001341550.1:n.-1029_-1016del | |
| NM_001354622.1:c.-1142_-1129del | NP_001341551.1:n.-1142_-1129del | |
| NM_001354623.1:c.-1051_-1038del | NP_001341552.1:n.-1051_-1038del | |
| NM_001354624.1:c.-812_-799del | NP_001341553.1:n.-812_-799del | |
| NM_001354625.1:c.-710_-697del | NP_001341554.1:n.-710_-697del | |
| NM_001354626.1:c.-807_-794del | NP_001341555.1:n.-807_-794del | |
| NM_001354627.1:c.-1039_-1026del | NP_001341556.1:n.-1039_-1026del | |
| NM_001354628.1:c.15_28del | NP_001341557.1:p.Gly6AlafsTer20 | |
| NM_001354629.1:c.15_28del | NP_001341558.1:p.Gly6AlafsTer20 | |
| NM_001354630.1:c.15_28del | NP_001341559.1:p.Gly6AlafsTer20 | |
| XM_005265161.2:c.15_28del | XP_005265218.1:p.Gly6AlafsTer20 | |
| XM_017006450.2:c.-797_-784del | XP_016861939.1:n.-797_-784del | |
| NM_000249.4:c.15_28del MANE Select | NP_000240.1:p.Gly6AlafsTer20 | |
| NM_001167617.3:c.-502_-489del | NP_001161089.1:n.-502_-489del | |
| NM_001167618.3:c.-931_-918del | NP_001161090.1:n.-931_-918del | |
| NM_001167619.3:c.-844_-831del | NP_001161091.1:n.-844_-831del | |
| NM_001258271.2:c.15_28del | NP_001245200.1:p.Gly6AlafsTer20 | |
| NM_001258273.2:c.-618_-605del | NP_001245202.1:n.-618_-605del | |
| NM_001258274.3:c.-1081_-1068del | NP_001245203.1:n.-1081_-1068del | |
| NM_001354615.2:c.-612_-599del | NP_001341544.1:n.-612_-599del | |
| NM_001354616.2:c.-612_-599del | NP_001341545.1:n.-612_-599del | |
| NM_001354617.2:c.-704_-691del | NP_001341546.1:n.-704_-691del | |
| NM_001354618.2:c.-936_-923del | NP_001341547.1:n.-936_-923del | |
| NM_001354619.2:c.-1060_-1047del | NP_001341548.1:n.-1060_-1047del | |
| NM_001354620.2:c.-270_-257del | NP_001341549.1:n.-270_-257del | |
| NM_001354621.2:c.-1029_-1016del | NP_001341550.1:n.-1029_-1016del | |
| NM_001354622.2:c.-1142_-1129del | NP_001341551.1:n.-1142_-1129del | |
| NM_001354623.2:c.-1051_-1038del | NP_001341552.1:n.-1051_-1038del | |
| NM_001354624.2:c.-812_-799del | NP_001341553.1:n.-812_-799del | |
| NM_001354625.2:c.-710_-697del | NP_001341554.1:n.-710_-697del | |
| NM_001354626.2:c.-807_-794del | NP_001341555.1:n.-807_-794del | |
| NM_001354627.2:c.-1039_-1026del | NP_001341556.1:n.-1039_-1026del | |
| NM_001354628.2:c.15_28del | NP_001341557.1:p.Gly6AlafsTer20 | |
| NM_001354629.2:c.15_28del | NP_001341558.1:p.Gly6AlafsTer20 | |
| NM_001354630.2:c.15_28del | NP_001341559.1:p.Gly6AlafsTer20 |