Linked Data
ClinVar Variation Id:
1745699
ClinVar RCV Id:
RCV002338291
gnomAD v4:
5-1293692-C-A
MyVariant Identifiers:
chr5:g.1293807C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1293692C>A , CM000667.2:g.1293692C>A | GRCh38 |
| NC_000005.9:g.1293807C>A , CM000667.1:g.1293807C>A | GRCh37 |
| NC_000005.8:g.1346807C>A | NCBI36 |
| NG_009265.1:g.6356G>T , LRG_343:g.6356G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310581.10:c.1194G>T MANE Select | ENSP00000309572.5:p.Gly398= | |
| ENST00000656021.1:c.1194G>T | ENSP00000499759.1:p.Gly398= | |
| ENST00000310581.9:c.1194G>T | ENSP00000309572.5:p.Gly398= | |
| ENST00000334602.10:c.1194G>T | ENSP00000334346.6:p.Gly398= | |
| ENST00000460137.6:c.1194G>T | ENSP00000425003.1:p.Gly398= | |
| ENST00000508104.2:c.1194G>T | ENSP00000426042.2:p.Gly398= | |
| NM_001193376.1:c.1194G>T | NP_001180305.1:p.Gly398= | |
| NM_198253.2:c.1194G>T , LRG_343t1:c.1194G>T | NP_937983.2:p.Gly398= | |
| NR_149162.1:n.1252G>T | ||
| NR_149163.1:n.1252G>T | ||
| NM_001193376.2:c.1194G>T | NP_001180305.1:p.Gly398= | |
| NM_198253.3:c.1194G>T MANE Select | NP_937983.2:p.Gly398= | |
| NR_149162.2:n.1273G>T | ||
| NR_149163.2:n.1273G>T | ||
| NM_001193376.3:c.1194G>T | NP_001180305.1:p.Gly398= | |
| NR_149162.3:n.1273G>T | ||
| NR_149163.3:n.1273G>T |