MyVariant.info:
GRCh37
chrX:g.148585719dup
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.149504191dup , CM000685.2:g.149504191dup | GRCh38 |
| NC_000023.10:g.148585721dup , CM000685.1:g.148585721dup | GRCh37 |
| NC_000023.9:g.148393625dup | NCBI36 |
| NG_011900.3:g.6146dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340855.11:c.208dup MANE Select | ENSP00000339801.6:p.His70ProfsTer29 | |
| ENST00000651111.1:c.-215-3152dup | ENSP00000498395.1:n.-215-3152dup | |
| ENST00000340855.10:c.208dup | ENSP00000339801.6:p.His70ProfsTer29 | |
| ENST00000370441.8:c.208dup | ENSP00000359470.4:p.His70ProfsTer29 | |
| ENST00000422081.6:c.-215-3152dup | ENSP00000477056.1:n.-215-3152dup | |
| ENST00000427113.2:n.770-1966dup | ||
| ENST00000428056.6:c.208dup | ENSP00000390241.2:p.His70ProfsTer29 | |
| ENST00000441880.1:n.114-17091dup | ||
| ENST00000464251.5:c.31dup | ENSP00000428980.1:p.His11ProfsTer29 | |
| ENST00000466323.5:c.208dup | ENSP00000418264.1:p.His70ProfsTer29 | |
| ENST00000521702.1:c.208dup | ENSP00000429745.1:p.His70ProfsTer? | |
| ENST00000523759.5:n.533-3152dup | ||
| NM_000202.6:c.208dup | NP_000193.1:p.His70ProfsTer29 | |
| NM_001166550.2:c.-19dup | NP_001160022.1:n.-19dup | |
| NM_006123.4:c.208dup | NP_006114.1:p.His70ProfsTer29 | |
| NR_104128.1:n.425dup | ||
| NM_000202.7:c.208dup | NP_000193.1:p.His70ProfsTer29 | |
| NM_001166550.3:c.-19dup | NP_001160022.1:n.-19dup | |
| NM_000202.8:c.208dup MANE Select | NP_000193.1:p.His70ProfsTer29 | |
| NM_001166550.4:c.-19dup | NP_001160022.1:n.-19dup | |
| NM_006123.5:c.208dup | NP_006114.1:p.His70ProfsTer29 | |
| NR_104128.2:n.377dup |