UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
ClinVar Variation Id:
380
ClinVar RCV Id:
RCV000000411
dbSNP Id:
rs137854543
gnomAD v4:
20-45897736-A-G
PubMed:
PMID:8514852
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.45897736A>G , CM000682.2:g.45897736A>G | GRCh38 |
| NC_000020.10:g.44526375A>G , CM000682.1:g.44526375A>G | GRCh37 |
| NC_000020.9:g.43959782A>G | NCBI36 |
| NG_008291.1:g.11785A>G | |
| NG_012115.1:g.19412T>C | |
| NG_012115.2:g.19412T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000480961.3:n.5123A>G | ||
| ENST00000484855.4:n.3741A>G | ||
| ENST00000493522.8:n.1551A>G | ||
| ENST00000606066.3:n.1675A>G | ||
| ENST00000606782.3:n.1305A>G | ||
| ENST00000607187.3:n.4108A>G | ||
| ENST00000607212.3:n.1395A>G | ||
| ENST00000607814.7:n.2935A>G | ||
| ENST00000677755.2:n.1604A>G | ||
| ENST00000678622.2:n.2277A>G | ||
| ENST00000678691.2:n.3432A>G | ||
| ENST00000678988.2:n.2562A>G | ||
| ENST00000679053.2:n.4108A>G | ||
| ENST00000679343.2:n.4447A>G | ||
| ENST00000684198.1:n.1601A>G | ||
| ENST00000372459.7:c.1184A>G | ENSP00000361537.2:p.Tyr395Cys | |
| ENST00000372484.8:c.1238A>G | ENSP00000361562.3:p.Tyr413Cys | |
| ENST00000484855.3:n.3741A>G | ||
| ENST00000493522.7:n.1551A>G | ||
| ENST00000606066.2:n.1323A>G | ||
| ENST00000607187.2:n.3622A>G | ||
| ENST00000607212.2:n.1395A>G | ||
| ENST00000607482.6:c.1184A>G | ENSP00000475524.2:p.Tyr395Cys | |
| ENST00000646241.3:c.1184A>G MANE Select | ENSP00000493613.2:p.Tyr395Cys | |
| ENST00000676597.1:c.1094-269A>G | ENSP00000503904.1:n.1094-269A>G | |
| ENST00000676967.1:c.*577A>G | ENSP00000502866.1:n.*577A>G | |
| ENST00000677394.1:c.1238A>G | ENSP00000504790.1:p.Tyr413Cys | |
| ENST00000677525.1:c.*1007A>G | ENSP00000504197.1:n.*1007A>G | |
| ENST00000677755.1:n.1604A>G | ||
| ENST00000678025.1:c.*1248A>G | ENSP00000503463.1:n.*1248A>G | |
| ENST00000678078.1:c.*549A>G | ENSP00000502993.1:n.*549A>G | |
| ENST00000678217.1:c.1768A>G | ENSP00000504109.1:n.1768A>G | |
| ENST00000678331.1:c.1089-269A>G | ENSP00000504524.1:n.1089-269A>G | |
| ENST00000678443.1:c.1165-269A>G | ENSP00000504006.1:n.1165-269A>G | |
| ENST00000678512.1:n.5547A>G | ||
| ENST00000678622.1:n.1905A>G | ||
| ENST00000678691.1:n.2893A>G | ||
| ENST00000678939.1:c.*523A>G | ENSP00000503404.1:n.*523A>G | |
| ENST00000678988.1:n.2562A>G | ||
| ENST00000679053.1:n.3736A>G | ||
| ENST00000679343.1:n.4068A>G | ||
| ENST00000191018.9:c.1184A>G | ENSP00000191018.5:p.Tyr395Cys | |
| ENST00000354880.9:c.1187A>G | ENSP00000346952.4:p.Tyr396Cys | |
| ENST00000372459.6:c.1184A>G | ENSP00000361537.2:p.Tyr395Cys | |
| ENST00000372484.7:c.1238A>G | ENSP00000361562.3:p.Tyr413Cys | |
| ENST00000484855.2:n.1356A>G | ||
| ENST00000493522.6:n.843A>G | ||
| ENST00000606000.1:n.111A>G | ||
| ENST00000606788.5:c.*549A>G | ENSP00000476235.1:n.*549A>G | |
| ENST00000607187.1:n.462A>G | ||
| NM_000308.2:c.1238A>G | NP_000299.2:p.Tyr413Cys | |
| NM_000308.3:c.1238A>G | NP_000299.2:p.Tyr413Cys | |
| NM_001127695.1:c.1184A>G | NP_001121167.1:p.Tyr395Cys | |
| NM_001127695.2:c.1184A>G | NP_001121167.1:p.Tyr395Cys | |
| NM_001167594.1:c.1187A>G | NP_001161066.1:p.Tyr396Cys | |
| NM_001167594.2:c.1187A>G | NP_001161066.1:p.Tyr396Cys | |
| NR_133656.1:n.2427A>G | ||
| NM_000308.4:c.1184A>G MANE Select | NP_000299.3:p.Tyr395Cys | |
| NM_001127695.3:c.1184A>G | NP_001121167.1:p.Tyr395Cys | |
| NM_001167594.3:c.1133A>G | NP_001161066.2:p.Tyr378Cys | |
| NR_133656.2:n.1236A>G |