Linked Data
ClinVar Variation Id:
39602
ClinVar RCV Id:
RCV000032802
dbSNP Id:
rs398123010
PubMed:
PMID:20547126
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.72034369T>C , CM000670.2:g.72034369T>C | GRCh38 |
| NC_000008.10:g.72946604T>C , CM000670.1:g.72946604T>C | GRCh37 |
| NC_000008.9:g.73109158T>C | NCBI36 |
| NG_033890.1:g.46216A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262209.5:c.2564A>G (TRPA1) MANE Select | ENSP00000262209.4:p.Asn855Ser | |
| ENST00000262209.4:c.2564A>G (TRPA1) | ENSP00000262209.4:p.Asn855Ser | |
| ENST00000519720.5:n.660A>G (TRPA1) | ||
| ENST00000523582.5:c.2120A>G (TRPA1) | ENSP00000428151.1:p.Asn707Ser | |
| NM_007332.2:c.2564A>G (TRPA1) | NP_015628.2:p.Asn855Ser | |
| NR_033651.1:n.434-18170T>C (MSC-AS1) | ||
| NR_033652.1:n.1029-18170T>C (MSC-AS1) | ||
| XM_011517624.1:c.2639A>G (TRPA1) | XP_011515926.1:p.Asn880Ser | |
| XM_011517625.1:c.2564A>G (TRPA1) | XP_011515927.1:p.Asn855Ser | |
| XM_011517624.2:c.2639A>G (TRPA1) | XP_011515926.1:p.Asn880Ser | |
| XM_011517625.2:c.2564A>G (TRPA1) | XP_011515927.1:p.Asn855Ser | |
| XM_017013946.1:c.2564A>G (TRPA1) | XP_016869435.1:p.Asn855Ser | |
| NM_007332.3:c.2564A>G (TRPA1) MANE Select | NP_015628.2:p.Asn855Ser |