Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21010226_21010229delinsCTCA , CM000664.2:g.21010226_21010229delinsCTCA | GRCh38 |
| NC_000002.11:g.21233098_21233101delinsCTCA , CM000664.1:g.21233098_21233101delinsCTCA | GRCh37 |
| NC_000002.10:g.21086603_21086606delinsCTCA | NCBI36 |
| NG_011793.1:g.38845_38848delinsTGAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.6639_6642delinsTGAG MANE Select | ENSP00000233242.1:p.Asp2213= | |
| ENST00000616098.4:c.6639_6642delinsTGAG | ENSP00000477990.1:p.Asp2213= | |
| NM_000384.2:c.6639_6642delinsTGAG | NP_000375.2:p.Asp2213= | |
| XM_011532809.1:c.5869+504_5869+507delinsTGAG | XP_011531111.1:n.5869+504_5869+507delinsTGAG | |
| NM_000384.3:c.6639_6642delinsTGAG MANE Select | NP_000375.3:p.Asp2213= |