Linked Data
dbSNP Id:
rs1566859663
gnomAD v2:
15-38591501-TCAAA-T
gnomAD v4:
15-38299300-TCAAA-T
MyVariant Identifiers:
chr15:g.38591502_38591505del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38299304_38299307del , CM000677.2:g.38299304_38299307del | GRCh38 |
| NC_000015.9:g.38591505_38591508del , CM000677.1:g.38591505_38591508del | GRCh37 |
| NC_000015.8:g.36378797_36378800del | NCBI36 |
| NG_008980.1:g.51454_51457del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.33-69_33-66del MANE Select | ENSP00000299084.4:n.33-69_33-66del | |
| ENST00000299084.8:c.33-69_33-66del | ENSP00000299084.4:n.33-69_33-66del | |
| ENST00000561205.1:n.371-69_371-66del | ||
| ENST00000561317.1:c.-31-69_-31-66del | ENSP00000453680.1:n.-31-69_-31-66del | |
| NM_152594.2:c.33-69_33-66del | NP_689807.1:n.33-69_33-66del | |
| XM_005254202.2:c.69-69_69-66del | XP_005254259.1:n.69-69_69-66del | |
| XM_005254203.3:c.-15-22937_-15-22934del | XP_005254260.1:n.-15-22937_-15-22934del | |
| XM_011521288.1:c.-31-69_-31-66del | XP_011519590.1:n.-31-69_-31-66del | |
| XM_011521289.1:c.-31-69_-31-66del | XP_011519591.1:n.-31-69_-31-66del | |
| XM_011521290.1:c.-31-69_-31-66del | XP_011519592.1:n.-31-69_-31-66del | |
| XM_005254202.3:c.69-69_69-66del | XP_005254259.1:n.69-69_69-66del | |
| XM_011521289.3:c.-31-69_-31-66del | XP_011519591.1:n.-31-69_-31-66del | |
| NM_152594.3:c.33-69_33-66del MANE Select | NP_689807.1:n.33-69_33-66del |