Linked Data
dbSNP Id:
rs781909894
ExAC:
X:154088662 GTAT / G
gnomAD v2:
X-154088662-GTAT-G
gnomAD v4:
X-154860387-GTAT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154860389_154860391del , CM000685.2:g.154860389_154860391del | GRCh38 |
| NC_000023.10:g.154088664_154088666del , CM000685.1:g.154088664_154088666del | GRCh37 |
| NC_000023.9:g.153741858_153741860del | NCBI36 |
| NG_011403.1:g.167334_167336del | |
| NG_011403.2:g.167334_167336del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6900+42_6900+44del MANE Select | ENSP00000353393.4:n.6900+42_6900+44del | |
| ENST00000644698.1:c.633+42_633+44del | ENSP00000495706.1:n.633+42_633+44del | |
| ENST00000330287.10:c.495+42_495+44del | ENSP00000327895.6:n.495+42_495+44del | |
| ENST00000360256.8:c.6900+42_6900+44del | ENSP00000353393.4:n.6900+42_6900+44del | |
| NM_000132.3:c.6900+42_6900+44del | NP_000123.1:n.6900+42_6900+44del | |
| NM_019863.2:c.495+42_495+44del | NP_063916.1:n.495+42_495+44del | |
| XM_011531126.1:c.6795+42_6795+44del | XP_011529428.1:n.6795+42_6795+44del | |
| NM_000132.4:c.6900+42_6900+44del MANE Select | NP_000123.1:n.6900+42_6900+44del | |
| NM_019863.3:c.495+42_495+44del | NP_063916.1:n.495+42_495+44del |