Linked Data
dbSNP Id:
rs767332297
gnomAD v2:
7-7848795-TA-T
gnomAD v3:
7-7809164-TA-T
gnomAD v4:
7-7809164-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.7809165del , CM000669.2:g.7809165del | GRCh38 |
| NC_000007.13:g.7848796del , CM000669.1:g.7848796del | GRCh37 |
| NC_000007.12:g.7815321del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682710.1:c.156+7422del MANE Select | ENSP00000507605.1:n.156+7422del | |
| ENST00000406829.2:n.168+7422del | ||
| ENST00000463725.5:n.396+7422del | ||
| ENST00000482067.3:n.247+7422del | ||
| ENST00000636849.1:c.156+7422del | ENSP00000489648.1:n.156+7422del | |
| ENST00000638342.1:c.156+7422del | ENSP00000491286.1:n.156+7422del | |
| ENST00000639110.1:c.156+7422del | ENSP00000491319.1:n.156+7422del | |
| ENST00000639343.1:c.*58+7422del | ENSP00000491077.1:n.*58+7422del | |
| NM_001302348.1:c.156+7422del | NP_001289277.1:n.156+7422del | |
| NM_001302349.1:c.156+7422del | NP_001289278.1:n.156+7422del | |
| NM_001302350.1:c.51+7422del | NP_001289279.1:n.51+7422del | |
| NM_001302348.2:c.156+7422del MANE Select | NP_001289277.1:n.156+7422del | |
| NM_001302349.2:c.156+7422del | NP_001289278.1:n.156+7422del | |
| NM_001302350.2:c.51+7422del | NP_001289279.1:n.51+7422del |