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:
9209
ClinVar RCV Id:
RCV000009789
dbSNP Id:
rs137852648
PubMed:
PMID:19329989
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30612107C>T , CM000669.2:g.30612107C>T | GRCh38 |
| NC_000007.13:g.30651723C>T , CM000669.1:g.30651723C>T | GRCh37 |
| NC_000007.12:g.30618248C>T | NCBI36 |
| NG_007942.1:g.22543C>T , LRG_243:g.22543C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000389266.8:c.893C>T MANE Select | ENSP00000373918.3:p.Pro298Leu | |
| ENST00000444666.6:c.893C>T | ENSP00000415447.2:p.Pro298Leu | |
| ENST00000470392.2:n.983C>T | ||
| ENST00000478124.6:n.956C>T | ||
| ENST00000485784.2:n.972C>T | ||
| ENST00000674616.1:c.*607C>T | ENSP00000502408.1:n.*607C>T | |
| ENST00000674643.1:c.893C>T | ENSP00000501636.1:p.Pro298Leu | |
| ENST00000674734.1:n.1389C>T | ||
| ENST00000674737.1:c.*231C>T | ENSP00000502464.1:n.*231C>T | |
| ENST00000674807.1:c.893C>T | ENSP00000502814.1:p.Pro298Leu | |
| ENST00000674815.1:c.524C>T | ENSP00000502799.1:p.Pro175Leu | |
| ENST00000674851.1:c.524C>T | ENSP00000502451.1:p.Pro175Leu | |
| ENST00000674969.1:n.2766C>T | ||
| ENST00000675051.1:c.692C>T | ENSP00000502296.1:p.Pro231Leu | |
| ENST00000675529.1:c.*763C>T | ENSP00000501655.1:n.*763C>T | |
| ENST00000675587.1:n.909C>T | ||
| ENST00000675651.1:c.893C>T | ENSP00000502513.1:p.Pro298Leu | |
| ENST00000675693.1:c.725C>T | ENSP00000502174.1:p.Pro242Leu | |
| ENST00000675810.1:c.791C>T | ENSP00000502743.1:p.Pro264Leu | |
| ENST00000675859.1:c.893C>T | ENSP00000502033.1:p.Pro298Leu | |
| ENST00000675863.1:n.901C>T | ||
| ENST00000675886.1:n.6933C>T | ||
| ENST00000676088.1:c.*835C>T | ENSP00000501884.1:n.*835C>T | |
| ENST00000676140.1:c.893C>T | ENSP00000502571.1:p.Pro298Leu | |
| ENST00000676164.1:c.*344C>T | ENSP00000501986.1:n.*344C>T | |
| ENST00000676210.1:c.*182C>T | ENSP00000502373.1:n.*182C>T | |
| ENST00000676259.1:c.*325C>T | ENSP00000501980.1:n.*325C>T | |
| ENST00000676403.1:c.893C>T | ENSP00000502681.1:p.Pro298Leu | |
| ENST00000389266.7:c.893C>T | ENSP00000373918.3:p.Pro298Leu | |
| ENST00000478124.5:n.931C>T | ||
| NM_001316772.1:c.731C>T | NP_001303701.1:p.Pro244Leu | |
| NM_002047.2:c.893C>T , LRG_243t1:c.893C>T | NP_002038.2:p.Pro298Leu | |
| NM_002047.3:c.893C>T | NP_002038.2:p.Pro298Leu | |
| XM_006715686.1:c.524C>T | XP_006715749.1:p.Pro175Leu | |
| XM_006715686.2:c.524C>T | XP_006715749.1:p.Pro175Leu | |
| NM_002047.4:c.893C>T MANE Select | NP_002038.2:p.Pro298Leu |