Linked Data
dbSNP Id:
rs1554117282
gnomAD v3:
5-168459271-A-AAAG
gnomAD v4:
5-168459271-A-AAAG
MyVariant Identifiers:
chr5:g.167886276_167886277insAAG (hg19)
chr5:g.168459271_168459272insAAG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.168459273_168459274insGAA , CM000667.2:g.168459273_168459274insGAA | GRCh38 |
| NC_000005.9:g.167886278_167886279insGAA , CM000667.1:g.167886278_167886279insGAA | GRCh37 |
| NC_000005.8:g.167818856_167818857insGAA | NCBI36 |
| NG_016712.1:g.172214_172215insGAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265293.9:c.2824-1377_2824-1376insGAA MANE Select | ENSP00000265293.4:n.2824-1377_2824-1376insGAA | |
| ENST00000265293.8:c.2824-1377_2824-1376insGAA | ENSP00000265293.4:n.2824-1377_2824-1376insGAA | |
| ENST00000393895.7:c.2708-1377_2708-1376insGAA | ||
| ENST00000521089.5:c.2824-1377_2824-1376insGAA | ENSP00000427772.1:n.2824-1377_2824-1376insGAA | |
| ENST00000522140.1:n.640-1377_640-1376insGAA | ||
| ENST00000524038.5:c.802-1377_802-1376insGAA | ENSP00000428084.1:n.802-1377_802-1376insGAA | |
| ENST00000524228.5:c.2153-1377_2153-1376insGAA | ||
| ENST00000619752.1:c.640-1377_640-1376insGAA | ENSP00000483898.1:n.640-1377_640-1376insGAA | |
| NM_001161661.1:c.2824-1377_2824-1376insGAA | NP_001155133.1:n.2824-1377_2824-1376insGAA | |
| NM_001161662.1:c.2824-1377_2824-1376insGAA | NP_001155134.1:n.2824-1377_2824-1376insGAA | |
| NM_015238.2:c.2824-1377_2824-1376insGAA | NP_056053.1:n.2824-1377_2824-1376insGAA | |
| XM_005265850.1:c.2839-1377_2839-1376insGAA | XP_005265907.1:n.2839-1377_2839-1376insGAA | |
| XM_005265853.1:c.2824-1377_2824-1376insGAA | XP_005265910.1:n.2824-1377_2824-1376insGAA | |
| XM_011534485.1:c.3022-1377_3022-1376insGAA | XP_011532787.1:n.3022-1377_3022-1376insGAA | |
| XM_011534486.1:c.3022-1377_3022-1376insGAA | XP_011532788.1:n.3022-1377_3022-1376insGAA | |
| XM_011534487.1:c.3007-1377_3007-1376insGAA | XP_011532789.1:n.3007-1377_3007-1376insGAA | |
| XM_011534488.1:c.3022-1377_3022-1376insGAA | XP_011532790.1:n.3022-1377_3022-1376insGAA | |
| XM_011534489.1:c.3007-1377_3007-1376insGAA | XP_011532791.1:n.3007-1377_3007-1376insGAA | |
| XM_011534490.1:c.3022-1377_3022-1376insGAA | XP_011532792.1:n.3022-1377_3022-1376insGAA | |
| XM_011534491.1:c.3007-1377_3007-1376insGAA | XP_011532793.1:n.3007-1377_3007-1376insGAA | |
| XM_005265853.2:c.2824-1377_2824-1376insGAA | XP_005265910.1:n.2824-1377_2824-1376insGAA | |
| XM_017009276.1:c.3007-1377_3007-1376insGAA | XP_016864765.1:n.3007-1377_3007-1376insGAA | |
| XM_017009278.1:c.2557-1377_2557-1376insGAA | XP_016864767.1:n.2557-1377_2557-1376insGAA | |
| NM_001161661.2:c.2824-1377_2824-1376insGAA | NP_001155133.1:n.2824-1377_2824-1376insGAA | |
| NM_001161662.2:c.2824-1377_2824-1376insGAA | NP_001155134.1:n.2824-1377_2824-1376insGAA | |
| NM_015238.3:c.2824-1377_2824-1376insGAA MANE Select | NP_056053.1:n.2824-1377_2824-1376insGAA |