Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202467609dup , CM000664.2:g.202467609dup | GRCh38 |
| NC_000002.11:g.203332332dup , CM000664.1:g.203332332dup | GRCh37 |
| NC_000002.10:g.203040577dup | NCBI36 |
| NG_009363.1:g.96283dup , LRG_712:g.96283dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374580.10:c.338dup MANE Select | ENSP00000363708.4:p.Tyr113Ter | |
| ENST00000638587.1:c.269dup | ENSP00000491062.1:p.Tyr90Ter | |
| ENST00000374574.2:c.338dup | ENSP00000363702.2:p.Tyr113Ter | |
| ENST00000374580.8:c.338dup | ENSP00000363708.4:p.Tyr113Ter | |
| ENST00000479069.1:n.245dup | ||
| NM_001204.6:c.338dup , LRG_712t1:c.338dup | NP_001195.2:p.Tyr113Ter | |
| XM_011511687.1:c.338dup | XP_011509989.1:p.Tyr113Ter | |
| XM_011511688.1:c.338dup | XP_011509990.1:p.Tyr113Ter | |
| NM_001204.7:c.338dup MANE Select | NP_001195.2:p.Tyr113Ter |