Linked Data
dbSNP Id:
rs768453160
ExAC:
5:148388595 TA / T
gnomAD v2:
5-148388595-TA-T
gnomAD v4:
5-149009032-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149009033del , CM000667.2:g.149009033del | GRCh38 |
| NC_000005.9:g.148388596del , CM000667.1:g.148388596del | GRCh37 |
| NC_000005.8:g.148368789del | NCBI36 |
| NG_007947.2:g.59142del , LRG_269:g.59142del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.3224-32del | ||
| ENST00000515425.6:c.3328-32del MANE Select | ENSP00000423660.1:n.3328-32del | |
| ENST00000675793.1:c.*2612-32del | ENSP00000502039.1:n.*2612-32del | |
| ENST00000323829.9:c.*2716-32del | ENSP00000313025.5:n.*2716-32del | |
| ENST00000504517.5:c.2858-32del | ENSP00000421779.1:n.2858-32del | |
| ENST00000504690.5:c.3328-32del | ENSP00000425627.1:n.3328-32del | |
| ENST00000510779.1:c.2378-32del | ||
| ENST00000512049.5:c.3307-32del | ENSP00000421860.1:n.3307-32del | |
| ENST00000515425.5:c.3328-32del | ENSP00000423660.1:n.3328-32del | |
| NM_024577.3:c.3328-32del , LRG_269t1:c.3328-32del | NP_078853.2:n.3328-32del | |
| NM_024577.4:c.3328-32del MANE Select | NP_078853.2:n.3328-32del |