Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152310865_152310866delinsGT , CM000663.2:g.152310865_152310866delinsGT | GRCh38 |
| NC_000001.10:g.152283341_152283342delinsGT , CM000663.1:g.152283341_152283342delinsGT | GRCh37 |
| NC_000001.9:g.150549965_150549966delinsGT | NCBI36 |
| NG_016190.1:g.19338_19339delinsAC , LRG_1028:g.19338_19339delinsAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.4020_4021delinsAC MANE Select | ENSP00000357789.1:p.Gly1340= | |
| ENST00000368799.1:c.4020_4021delinsAC | ENSP00000357789.1:p.Gly1340= | |
| NM_002016.1:c.4020_4021delinsAC , LRG_1028t1:c.4020_4021delinsAC | NP_002007.1:p.Gly1340= | |
| XM_011509329.1:c.4020_4021delinsAC | XP_011507631.1:p.Gly1340= | |
| NM_002016.2:c.4020_4021delinsAC MANE Select | NP_002007.1:p.Gly1340= |