Linked Data
dbSNP Id:
rs1567510914
gnomAD v2:
16-68853350-CT-C
gnomAD v3:
16-68819447-CT-C
gnomAD v4:
16-68819447-CT-C
MyVariant Identifiers:
chr16:g.68853351del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68819450del , CM000678.2:g.68819450del | GRCh38 |
| NC_000016.9:g.68853353del , CM000678.1:g.68853353del | GRCh37 |
| NC_000016.8:g.67410854del | NCBI36 |
| NG_008021.1:g.87159del , LRG_301:g.87159del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.1711+25del MANE Select | ENSP00000261769.4:n.1711+25del | |
| ENST00000261769.9:c.1711+25del | ENSP00000261769.4:n.1711+25del | |
| ENST00000422392.6:c.1528+25del | ENSP00000414946.2:n.1528+25del | |
| ENST00000562836.5:n.1782+25del | ||
| ENST00000566510.5:c.*377+25del | ENSP00000458139.1:n.*377+25del | |
| ENST00000566612.5:c.1566-2551del | ENSP00000454782.1:n.1566-2551del | |
| ENST00000611625.4:c.1774+25del | ENSP00000481063.1:n.1774+25del | |
| ENST00000612417.4:c.1711+25del | ENSP00000478360.1:n.1711+25del | |
| ENST00000621016.4:c.1711+25del | ENSP00000480664.1:n.1711+25del | |
| NM_004360.3:c.1711+25del , LRG_301t1:c.1711+25del | NP_004351.1:n.1711+25del | |
| XM_011523488.1:c.976+25del | XP_011521790.1:n.976+25del | |
| XM_011523489.1:c.976+25del | XP_011521791.1:n.976+25del | |
| NM_001317184.1:c.1528+25del | NP_001304113.1:n.1528+25del | |
| NM_001317185.1:c.163+25del | NP_001304114.1:n.163+25del | |
| NM_001317186.1:c.-254-2551del | NP_001304115.1:n.-254-2551del | |
| NM_004360.4:c.1711+25del | NP_004351.1:n.1711+25del | |
| NM_004360.5:c.1711+25del MANE Select | NP_004351.1:n.1711+25del | |
| NM_001317184.2:c.1528+25del | NP_001304113.1:n.1528+25del | |
| NM_001317185.2:c.163+25del | NP_001304114.1:n.163+25del | |
| NM_001317186.2:c.-254-2551del | NP_001304115.1:n.-254-2551del |