Linked Data
gnomAD v4:
21-45990485-G-GCA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990485_45990486insCA , CM000683.2:g.45990485_45990486insCA | GRCh38 |
| NC_000021.8:g.47410399_47410400insCA , CM000683.1:g.47410399_47410400insCA | GRCh37 |
| NC_000021.7:g.46234827_46234828insCA | NCBI36 |
| NG_008674.1:g.13737_13738insCA , LRG_475:g.13737_13738insCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1002+63_1002+64insCA MANE Select | ENSP00000355180.3:n.1002+63_1002+64insCA | |
| ENST00000361866.7:c.1002+63_1002+64insCA | ENSP00000355180.3:n.1002+63_1002+64insCA | |
| ENST00000612273.1:c.1002+63_1002+64insCA | ENSP00000483630.1:n.1002+63_1002+64insCA | |
| NM_001848.2:c.1002+63_1002+64insCA , LRG_475t1:c.1002+63_1002+64insCA | NP_001839.2:n.1002+63_1002+64insCA | |
| NM_001848.3:c.1002+63_1002+64insCA MANE Select | NP_001839.2:n.1002+63_1002+64insCA |