Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.61378526_61378530delinsCAATA , CM000664.2:g.61378526_61378530delinsCAATA | GRCh38 |
| NC_000002.11:g.61605661_61605665delinsCAATA , CM000664.1:g.61605661_61605665delinsCAATA | GRCh37 |
| NC_000002.10:g.61459165_61459169delinsCAATA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398571.7:c.1015-106_1015-102delinsTATTG MANE Select | ENSP00000381577.2:n.1015-106_1015-102delinsTATTG | |
| ENST00000398571.6:c.1015-106_1015-102delinsTATTG | ENSP00000381577.2:n.1015-106_1015-102delinsTATTG | |
| ENST00000453133.1:c.541-106_541-102delinsTATTG | ||
| NM_014709.3:c.1015-106_1015-102delinsTATTG | NP_055524.3:n.1015-106_1015-102delinsTATTG | |
| NM_014709.4:c.1015-106_1015-102delinsTATTG MANE Select | NP_055524.3:n.1015-106_1015-102delinsTATTG |