Linked Data
dbSNP Id:
rs749117806
gnomAD v2:
5-148388589-TTAGTCTAGC-T
gnomAD v3:
5-149009026-TTAGTCTAGC-T
gnomAD v4:
5-149009026-TTAGTCTAGC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149009030_149009038del , CM000667.2:g.149009030_149009038del | GRCh38 |
| NC_000005.9:g.148388593_148388601del , CM000667.1:g.148388593_148388601del | GRCh37 |
| NC_000005.8:g.148368786_148368794del | NCBI36 |
| NG_007947.2:g.59140_59148del , LRG_269:g.59140_59148del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.3224-34_3224-26del | ||
| ENST00000515425.6:c.3328-34_3328-26del MANE Select | ENSP00000423660.1:n.3328-34_3328-26del | |
| ENST00000675793.1:c.*2612-34_*2612-26del | ENSP00000502039.1:n.*2612-34_*2612-26del | |
| ENST00000323829.9:c.*2716-34_*2716-26del | ENSP00000313025.5:n.*2716-34_*2716-26del | |
| ENST00000504517.5:c.2858-34_2858-26del | ENSP00000421779.1:n.2858-34_2858-26del | |
| ENST00000504690.5:c.3328-34_3328-26del | ENSP00000425627.1:n.3328-34_3328-26del | |
| ENST00000510779.1:c.2378-34_2378-26del | ||
| ENST00000512049.5:c.3307-34_3307-26del | ENSP00000421860.1:n.3307-34_3307-26del | |
| ENST00000515425.5:c.3328-34_3328-26del | ENSP00000423660.1:n.3328-34_3328-26del | |
| NM_024577.3:c.3328-34_3328-26del , LRG_269t1:c.3328-34_3328-26del | NP_078853.2:n.3328-34_3328-26del | |
| NM_024577.4:c.3328-34_3328-26del MANE Select | NP_078853.2:n.3328-34_3328-26del |