Linked Data
dbSNP Id:
rs12032481
gnomAD v2:
1-243788009-A-C
gnomAD v3:
1-243624707-A-C
gnomAD v4:
1-243624707-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.243624707A>C , CM000663.2:g.243624707A>C | GRCh38 |
| NC_000001.10:g.243788009A>C , CM000663.1:g.243788009A>C | GRCh37 |
| NC_000001.9:g.241854632A>C | NCBI36 |
| NG_029764.1:g.223878T>G | |
| NG_029764.2:g.231373T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263826.12:c.562-9546T>G (AKT3) | ENSP00000263826.5:n.562-9546T>G | |
| ENST00000366539.6:c.562-9546T>G (AKT3) | ENSP00000355497.2:n.562-9546T>G | |
| ENST00000492957.2:c.562-9546T>G (AKT3) | ENSP00000506695.1:n.562-9546T>G | |
| ENST00000672460.1:c.319-9546T>G (AKT3) | ENSP00000499842.1:n.319-9546T>G | |
| ENST00000672578.1:c.379-9546T>G (AKT3) | ENSP00000500597.1:n.379-9546T>G | |
| ENST00000673466.1:c.562-9546T>G (AKT3) MANE Select | ENSP00000500582.1:n.562-9546T>G | |
| ENST00000680056.1:c.436-9546T>G (AKT3) | ENSP00000505337.1:n.436-9546T>G | |
| ENST00000680118.1:c.562-9546T>G (AKT3) | ENSP00000505276.1:n.562-9546T>G | |
| ENST00000681794.1:c.562-9546T>G (AKT3) | ENSP00000506399.1:n.562-9546T>G | |
| ENST00000263826.9:c.562-9546T>G (AKT3) | ENSP00000263826.5:n.562-9546T>G | |
| ENST00000336199.9:c.562-9546T>G (AKT3) | ENSP00000336943.5:n.562-9546T>G | |
| ENST00000366539.5:c.562-9546T>G (AKT3) | ENSP00000355497.1:n.562-9546T>G | |
| ENST00000366540.5:c.562-9546T>G (AKT3) | ENSP00000355498.1:n.562-9546T>G | |
| ENST00000424004.1:n.350T>G (FABP7P1) | ||
| NM_001206729.1:c.562-9546T>G (AKT3) | NP_001193658.1:n.562-9546T>G | |
| NM_005465.4:c.562-9546T>G (AKT3) | NP_005456.1:n.562-9546T>G | |
| NM_181690.2:c.562-9546T>G (AKT3) | NP_859029.1:n.562-9546T>G | |
| XM_005272994.3:c.562-9546T>G (AKT3) | XP_005273051.1:n.562-9546T>G | |
| XM_005272995.2:c.562-9546T>G (AKT3) | XP_005273052.1:n.562-9546T>G | |
| XM_005272997.3:c.379-9546T>G (AKT3) | XP_005273054.1:n.379-9546T>G | |
| XM_006711726.2:c.562-9546T>G (AKT3) | XP_006711789.1:n.562-9546T>G | |
| XM_011544011.1:c.436-9546T>G (AKT3) | XP_011542313.1:n.436-9546T>G | |
| XM_011544012.1:c.562-9546T>G (AKT3) | XP_011542314.1:n.562-9546T>G | |
| XM_011544013.1:c.562-9546T>G (AKT3) | XP_011542315.1:n.562-9546T>G | |
| XM_016999985.1:c.379-9546T>G (AKT3) | XP_016855474.1:n.379-9546T>G | |
| XM_024446000.1:c.562-9546T>G (AKT3) | XP_024301768.1:n.562-9546T>G | |
| XM_024446892.1:c.562-9546T>G (AKT3) | XP_024302660.1:n.562-9546T>G | |
| XM_024447938.1:c.562-9546T>G (AKT3) | XP_024303706.1:n.562-9546T>G | |
| NM_005465.5:c.562-9546T>G (AKT3) | NP_005456.1:n.562-9546T>G | |
| NM_001370074.1:c.562-9546T>G (AKT3) | NP_001357003.1:n.562-9546T>G | |
| NM_005465.7:c.562-9546T>G (AKT3) MANE Select | NP_005456.1:n.562-9546T>G | |
| NM_001206729.2:c.562-9546T>G (AKT3) | NP_001193658.1:n.562-9546T>G |