Linked Data
ClinVar Variation Id:
302505
dbSNP Id:
rs574061789
ExAC:
11:116706874 C / T
gnomAD v2:
11-116706874-C-T
gnomAD v3:
11-116836158-C-T
gnomAD v4:
11-116836158-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116836158C>T , CM000673.2:g.116836158C>T | GRCh38 |
| NC_000011.9:g.116706874C>T , CM000673.1:g.116706874C>T | GRCh37 |
| NC_000011.8:g.116212084C>T | NCBI36 |
| NG_012021.1:g.6465G>A , LRG_767:g.6465G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000236850.5:c.454G>A (APOA1) MANE Select | ENSP00000236850.3:p.Glu152Lys | |
| ENST00000236850.4:c.454G>A (APOA1) | ENSP00000236850.3:p.Glu152Lys | |
| ENST00000359492.6:c.454G>A (APOA1) | ENSP00000352471.2:p.Glu152Lys | |
| ENST00000375320.5:c.454G>A (APOA1) | ENSP00000364469.1:p.Glu152Lys | |
| ENST00000375323.5:c.454G>A (APOA1) | ENSP00000364472.1:p.Glu152Lys | |
| ENST00000375329.6:c.388G>A (APOA1) | ENSP00000364478.2:p.Glu130Lys | |
| NM_000039.1:c.454G>A , LRG_767t1:c.454G>A (APOA1) | NP_000030.1:p.Glu152Lys | |
| NR_126362.1:n.42C>T (APOA1-AS) | ||
| XM_005271539.2:c.454G>A (APOA1) | XP_005271596.1:p.Glu152Lys | |
| XM_005271540.1:c.454G>A (APOA1) | XP_005271597.1:p.Glu152Lys | |
| NM_000039.2:c.454G>A (APOA1) | NP_000030.1:p.Glu152Lys | |
| NM_001318017.1:c.454G>A (APOA1) | NP_001304946.1:p.Glu152Lys | |
| NM_001318018.1:c.454G>A (APOA1) | NP_001304947.1:p.Glu152Lys | |
| NM_001318021.1:c.127G>A (APOA1) | NP_001304950.1:p.Glu43Lys | |
| NM_001318017.2:c.454G>A (APOA1) | NP_001304946.1:p.Glu152Lys | |
| NM_001318018.2:c.454G>A (APOA1) | NP_001304947.1:p.Glu152Lys | |
| NM_000039.3:c.454G>A (APOA1) MANE Select | NP_000030.1:p.Glu152Lys |