Linked Data
dbSNP Id:
rs1231350621
gnomAD v3:
12-102865643-ATCCTGCTCAGC-A
gnomAD v4:
12-102865643-ATCCTGCTCAGC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102865644_102865654del , CM000674.2:g.102865644_102865654del | GRCh38 |
| NC_000012.11:g.103259422_103259432del , CM000674.1:g.103259422_103259432del | GRCh37 |
| NC_000012.10:g.101783552_101783562del | NCBI36 |
| NG_008690.1:g.56949_56959del | |
| NG_008690.2:g.97757_97767del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.509+942_509+952del MANE Select | ENSP00000448059.1:n.509+942_509+952del | |
| ENST00000307000.7:c.494+942_494+952del | ENSP00000303500.2:n.494+942_494+952del | |
| ENST00000549111.5:n.605+942_605+952del | ||
| ENST00000551988.5:n.531-10322_531-10312del | ||
| ENST00000553106.5:c.509+942_509+952del | ENSP00000448059.1:n.509+942_509+952del | |
| NM_000277.1:c.509+942_509+952del | NP_000268.1:n.509+942_509+952del | |
| XM_011538422.1:c.509+942_509+952del | XP_011536724.1:n.509+942_509+952del | |
| NM_000277.2:c.509+942_509+952del | NP_000268.1:n.509+942_509+952del | |
| NM_001354304.1:c.509+942_509+952del | NP_001341233.1:n.509+942_509+952del | |
| XM_017019370.2:c.509+942_509+952del | XP_016874859.1:n.509+942_509+952del | |
| NM_000277.3:c.509+942_509+952del MANE Select | NP_000268.1:n.509+942_509+952del | |
| NM_001354304.2:c.509+942_509+952del | NP_001341233.1:n.509+942_509+952del |