Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35842036_35842120del , CM000681.2:g.35842036_35842120del | GRCh38 |
| NC_000019.9:g.36332938_36333022del , CM000681.1:g.36332938_36333022del | GRCh37 |
| NC_000019.8:g.41024778_41024862del | NCBI36 |
| NG_013356.2:g.32170_32254del , LRG_693:g.32170_32254del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.2663+6_2663+90del MANE Select | ENSP00000368190.4:n.2663+6_2663+90del | |
| ENST00000353632.6:c.2663+6_2663+90del | ENSP00000343634.5:n.2663+6_2663+90del | |
| ENST00000378910.9:c.2663+6_2663+90del | ENSP00000368190.4:n.2663+6_2663+90del | |
| NM_004646.3:c.2663+6_2663+90del , LRG_693t1:c.2663+6_2663+90del | NP_004637.1:n.2663+6_2663+90del | |
| NM_004646.4:c.2663+6_2663+90del MANE Select | NP_004637.1:n.2663+6_2663+90del |