Linked Data
ClinVar Variation Id:
1186418
ClinVar RCV Id:
RCV001545502
dbSNP Id:
rs200871280
ExAC:
11:121016511 A / G
gnomAD v2:
11-121016511-A-G
gnomAD v3:
11-121145802-A-G
gnomAD v4:
11-121145802-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121145802A>G , CM000673.2:g.121145802A>G | GRCh38 |
| NC_000011.9:g.121016511A>G , CM000673.1:g.121016511A>G | GRCh37 |
| NC_000011.8:g.120521721A>G | NCBI36 |
| NG_011633.1:g.48137A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392793.6:c.3791A>G (TECTA) MANE Select | ENSP00000376543.1:p.Asn1264Ser | |
| ENST00000642222.1:c.3791A>G (TECTA) | ENSP00000493855.1:p.Asn1264Ser | |
| ENST00000645008.1:c.1098A>G (TECTA) | ||
| ENST00000264037.2:c.3791A>G (TECTA) | ENSP00000264037.2:p.Asn1264Ser | |
| ENST00000392793.5:c.3791A>G (TECTA) | ENSP00000376543.1:p.Asn1264Ser | |
| ENST00000478058.1:n.356A>G (TECTA) | ||
| NM_005422.2:c.3791A>G (TECTA) | NP_005413.2:p.Asn1264Ser | |
| NM_001378761.1:c.4748A>G (TBCEL-TECTA) | NP_001365690.1:p.Asn1583Ser | |
| NM_005422.4:c.3791A>G (TECTA) MANE Select | NP_005413.2:p.Asn1264Ser |