Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.55811860_55811862delinsTAC , CM000673.2:g.55811860_55811862delinsTAC | GRCh38 |
| NC_000011.9:g.55579336_55579338delinsTAC , CM000673.1:g.55579336_55579338delinsTAC | GRCh37 |
| NC_000011.8:g.55335912_55335914delinsTAC | NCBI36 |
| NG_052620.1:g.5494_5496delinsTAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000625203.2:c.394_396delinsTAC MANE Select | ENSP00000485319.1:p.Tyr132= | |
| ENST00000333973.3:c.394_396delinsTAC | ENSP00000335529.2:p.Tyr132= | |
| ENST00000623450.1:c.394_396delinsTAC | ENSP00000485509.1:p.Tyr132= | |
| ENST00000625203.1:c.394_396delinsTAC | ENSP00000485319.1:p.Tyr132= | |
| NM_001004738.1:c.394_396delinsTAC | NP_001004738.1:p.Tyr132= | |
| NM_001004738.2:c.394_396delinsTAC MANE Select | NP_001004738.1:p.Tyr132= |