Linked Data
dbSNP Id:
rs979608472
MyVariant Identifiers:
chr4:g.187209231_187209232insTC (hg19)
chr4:g.186288077_186288078insTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186288078_186288079insCT , CM000666.2:g.186288078_186288079insCT | GRCh38 |
| NC_000004.11:g.187209232_187209233insCT , CM000666.1:g.187209232_187209233insCT | GRCh37 |
| NC_000004.10:g.187446226_187446227insCT | NCBI36 |
| NG_008051.1:g.27115_27116insCT , LRG_583:g.27115_27116insCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403665.7:c.1716+255_1716+256insCT (F11) MANE Select | ENSP00000384957.2:n.1716+255_1716+256insCT | |
| ENST00000264691.4:c.316+255_316+256insCT (F11) | ||
| ENST00000264692.8:c.1554+255_1554+256insCT (F11) | ENSP00000264692.5:n.1554+255_1554+256insCT | |
| ENST00000403665.6:c.1716+255_1716+256insCT (F11) | ENSP00000384957.2:n.1716+255_1716+256insCT | |
| ENST00000503841.1:n.235+255_235+256insCT (F11) | ||
| NM_000128.3:c.1716+255_1716+256insCT , LRG_583t1:c.1716+255_1716+256insCT (F11) | NP_000119.1:n.1716+255_1716+256insCT | |
| NR_033900.1:n.1066+350_1066+351insGA (F11-AS1) | ||
| XM_005262821.2:c.1719+255_1719+256insCT (F11) | XP_005262878.1:n.1719+255_1719+256insCT | |
| XM_005262822.2:c.1623+255_1623+256insCT (F11) | XP_005262879.1:n.1623+255_1623+256insCT | |
| XM_005262823.2:c.1449+255_1449+256insCT (F11) | XP_005262880.1:n.1449+255_1449+256insCT | |
| XM_006714137.1:c.1671+255_1671+256insCT (F11) | XP_006714200.1:n.1671+255_1671+256insCT | |
| XM_005262821.4:c.1719+255_1719+256insCT (F11) | XP_005262878.1:n.1719+255_1719+256insCT | |
| XM_005262822.4:c.1623+255_1623+256insCT (F11) | XP_005262879.1:n.1623+255_1623+256insCT | |
| XM_005262823.4:c.1449+255_1449+256insCT (F11) | XP_005262880.1:n.1449+255_1449+256insCT | |
| XM_006714137.3:c.1671+255_1671+256insCT (F11) | XP_006714200.1:n.1671+255_1671+256insCT | |
| NM_000128.4:c.1716+255_1716+256insCT (F11) MANE Select | NP_000119.1:n.1716+255_1716+256insCT |