Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1414408_1414409delinsTG , CM000667.2:g.1414408_1414409delinsTG | GRCh38 |
| NC_000005.9:g.1414523_1414524delinsTG , CM000667.1:g.1414523_1414524delinsTG | GRCh37 |
| NC_000005.8:g.1467523_1467524delinsTG | NCBI36 |
| NG_015885.1:g.36020_36021delinsCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1156+282_1156+283delinsCA MANE Select | ENSP00000270349.9:n.1156+282_1156+283delinsCA | |
| ENST00000270349.11:c.1156+282_1156+283delinsCA | ENSP00000270349.9:n.1156+282_1156+283delinsCA | |
| NM_001044.4:c.1156+282_1156+283delinsCA | NP_001035.1:n.1156+282_1156+283delinsCA | |
| NM_001044.5:c.1156+282_1156+283delinsCA MANE Select | NP_001035.1:n.1156+282_1156+283delinsCA |