Linked Data
dbSNP Id:
rs1334407341
gnomAD v2:
2-26690316-TCTC-T
gnomAD v3:
2-26467448-TCTC-T
gnomAD v4:
2-26467448-TCTC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26467452_26467454del , CM000664.2:g.26467452_26467454del | GRCh38 |
| NC_000002.11:g.26690320_26690322del , CM000664.1:g.26690320_26690322del | GRCh37 |
| NC_000002.10:g.26543824_26543826del | NCBI36 |
| NG_009937.1:g.96248_96250del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272371.7:c.4141_4143del MANE Select | ENSP00000272371.2:p.Glu1381del | |
| ENST00000339598.8:c.1840_1842del MANE Plus Clinical | ENSP00000344521.3:p.Glu614del | |
| ENST00000402415.8:c.1900_1902del | ENSP00000383906.4:p.Glu634del | |
| ENST00000272371.6:c.4141_4143del | ENSP00000272371.2:p.Glu1381del | |
| ENST00000338581.10:c.1840_1842del | ENSP00000345137.6:p.Glu614del | |
| ENST00000339598.7:c.1840_1842del | ENSP00000344521.3:p.Glu614del | |
| ENST00000402415.7:c.2071_2073del | ENSP00000383906.3:p.Glu691del | |
| ENST00000403946.7:c.4141_4143del | ENSP00000385255.3:p.Glu1381del | |
| NM_001287489.1:c.4141_4143del | NP_001274418.1:p.Glu1381del | |
| NM_004802.3:c.1840_1842del | NP_004793.2:p.Glu614del | |
| NM_194248.2:c.4141_4143del | NP_919224.1:p.Glu1381del | |
| NM_194322.2:c.2071_2073del | NP_919303.1:p.Glu691del | |
| NM_194323.2:c.1840_1842del | NP_919304.1:p.Glu614del | |
| XM_005264644.2:c.4126_4128del | XP_005264701.1:p.Glu1376del | |
| XM_011533185.1:c.4186_4188del | XP_011531487.1:p.Glu1396del | |
| XM_017005338.1:c.4081_4083del | XP_016860827.1:p.Glu1361del | |
| NM_001287489.2:c.4141_4143del | NP_001274418.1:p.Glu1381del | |
| NM_004802.4:c.1840_1842del | NP_004793.2:p.Glu614del | |
| NM_194248.3:c.4141_4143del MANE Select | NP_919224.1:p.Glu1381del | |
| NM_194322.3:c.2071_2073del | NP_919303.1:p.Glu691del | |
| NM_194323.3:c.1840_1842del MANE Plus Clinical | NP_919304.1:p.Glu614del |