Linked Data
MyVariant Identifiers:
chrX:g.154132218_154132219insA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154903943_154903944insA , CM000685.2:g.154903943_154903944insA | GRCh38 |
| NC_000023.10:g.154132218_154132219insA , CM000685.1:g.154132218_154132219insA | GRCh37 |
| NC_000023.9:g.153785412_153785413insA | NCBI36 |
| NG_011403.1:g.123780_123781insT | |
| NG_011403.2:g.123780_123781insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5960_5961insT MANE Select | ENSP00000353393.4:p.Lys1987AsnfsTer5 | |
| ENST00000360256.8:c.5960_5961insT | ENSP00000353393.4:p.Lys1987AsnfsTer5 | |
| NM_000132.3:c.5960_5961insT | NP_000123.1:p.Lys1987AsnfsTer5 | |
| XM_011531126.1:c.5855_5856insT | XP_011529428.1:p.Lys1952AsnfsTer5 | |
| NM_000132.4:c.5960_5961insT MANE Select | NP_000123.1:p.Lys1987AsnfsTer5 |