Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816753T= , CM000681.2:g.4816753T= | GRCh38 |
| NC_000019.9:g.4816765T= , CM000681.1:g.4816765T= | GRCh37 |
| NC_000019.8:g.4767765T= | NCBI36 |
| NG_031998.1:g.19990A= , LRG_358:g.19990A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1625A= MANE Select | ENSP00000248244.4:p.Lys542= | |
| ENST00000248244.5:c.1625A= | ENSP00000248244.4:p.Lys542= | |
| ENST00000621756.1:c.1208A= | ENSP00000479467.1:p.Lys403= | |
| NM_182919.3:c.1625A= , LRG_358t1:c.1625A= | NP_891549.1:p.Lys542= | |
| NM_001385678.1:c.1583A= | NP_001372607.1:p.Lys528= | |
| NM_001385679.1:c.1490A= | NP_001372608.1:p.Lys497= | |
| NM_001385680.1:c.983A= | NP_001372609.1:p.Lys328= | |
| NM_182919.4:c.1625A= MANE Select | NP_891549.1:p.Lys542= |