Linked Data
dbSNP Id:
rs761419877
gnomAD v3:
X-108440271-T-TTG
gnomAD v4:
X-108440271-T-TTG
MyVariant Identifiers:
chrX:g.107683501_107683502insTG (hg19)
chrX:g.108440271_108440272insTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108440271_108440272insTG , CM000685.2:g.108440271_108440272insTG | GRCh38 |
| NC_000023.10:g.107683501_107683502insTG , CM000685.1:g.107683501_107683502insTG | GRCh37 |
| NC_000023.9:g.107570157_107570158insTG | NCBI36 |
| NG_011977.1:g.5348_5349insTG | |
| NG_012059.2:g.4203_4204insCA | |
| NG_011977.2:g.5348_5349insTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328300.11:c.81+65_81+66insTG MANE Select | ENSP00000331902.7:n.81+65_81+66insTG | |
| ENST00000361603.7:c.81+65_81+66insTG | ENSP00000354505.2:n.81+65_81+66insTG | |
| ENST00000642185.1:c.81+65_81+66insTG | ENSP00000495101.1:n.81+65_81+66insTG | |
| ENST00000328300.10:c.81+65_81+66insTG | ENSP00000331902.6:n.81+65_81+66insTG | |
| ENST00000361603.6:c.81+65_81+66insTG | ENSP00000354505.2:n.81+65_81+66insTG | |
| ENST00000470339.1:n.265+65_265+66insTG | ||
| ENST00000477429.1:n.363+65_363+66insTG | ||
| NM_000495.4:c.81+65_81+66insTG | NP_000486.1:n.81+65_81+66insTG | |
| NM_033380.2:c.81+65_81+66insTG | NP_203699.1:n.81+65_81+66insTG | |
| XM_005262070.2:c.81+65_81+66insTG | XP_005262127.1:n.81+65_81+66insTG | |
| XM_005262072.3:c.81+65_81+66insTG | XP_005262129.1:n.81+65_81+66insTG | |
| XM_006724616.2:c.81+65_81+66insTG | XP_006724679.1:n.81+65_81+66insTG | |
| XM_011530850.1:c.81+65_81+66insTG | XP_011529152.1:n.81+65_81+66insTG | |
| NM_000495.5:c.81+65_81+66insTG | NP_000486.1:n.81+65_81+66insTG | |
| NM_033380.3:c.81+65_81+66insTG MANE Select | NP_203699.1:n.81+65_81+66insTG |