Linked Data
dbSNP Id:
rs1390669621
gnomAD v4:
14-65471138-G-GAGATC
MyVariant Identifiers:
chr14:g.65937856_65937857insAGATC (hg19)
chr14:g.65471138_65471139insAGATC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65471138_65471139insAGATC , CM000676.2:g.65471138_65471139insAGATC | GRCh38 |
| NC_000014.8:g.65937856_65937857insAGATC , CM000676.1:g.65937856_65937857insAGATC | GRCh37 |
| NC_000014.7:g.65007609_65007610insAGATC | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673929.1:c.-228+15420_-228+15421insAGATC (FUT8) MANE Select | ENSP00000501213.1:n.-228+15420_-228+15421insAGATC | |
| ENST00000674118.1:c.-228+15420_-228+15421insAGATC (FUT8) | ENSP00000501008.1:n.-228+15420_-228+15421insAGATC | |
| ENST00000342677.10:c.-228+15420_-228+15421insAGATC (FUT8) | ENSP00000345865.6:n.-228+15420_-228+15421insAGATC | |
| ENST00000358307.6:c.-287+15420_-287+15421insAGATC (FUT8) | ENSP00000351057.2:n.-287+15420_-287+15421insAGATC | |
| ENST00000360689.9:c.-228+15420_-228+15421insAGATC (FUT8) | ENSP00000353910.5:n.-228+15420_-228+15421insAGATC | |
| ENST00000394586.6:c.-228+59145_-228+59146insAGATC (FUT8) | ENSP00000378087.2:n.-228+59145_-228+59146insAGATC | |
| ENST00000553924.5:c.-374+15420_-374+15421insAGATC (FUT8) | ENSP00000451577.1:n.-374+15420_-374+15421insAGATC | |
| ENST00000554610.1:c.-228+57924_-228+57925insAGATC (FUT8) | ENSP00000452309.1:n.-228+57924_-228+57925insAGATC | |
| ENST00000555559.5:c.-305-8569_-305-8568insAGATC (FUT8) | ENSP00000451689.1:n.-305-8569_-305-8568insAGATC | |
| ENST00000556518.5:c.-228+15420_-228+15421insAGATC (FUT8) | ENSP00000452597.1:n.-228+15420_-228+15421insAGATC | |
| ENST00000557164.5:c.-287+15420_-287+15421insAGATC (FUT8) | ENSP00000452433.1:n.-287+15420_-287+15421insAGATC | |
| ENST00000557338.5:c.-305-8569_-305-8568insAGATC (FUT8) | ENSP00000452105.1:n.-305-8569_-305-8568insAGATC | |
| NM_004480.4:c.-287+15420_-287+15421insAGATC (FUT8) | NP_004471.4:n.-287+15420_-287+15421insAGATC | |
| NM_178155.2:c.-228+15420_-228+15421insAGATC (FUT8) | NP_835368.1:n.-228+15420_-228+15421insAGATC | |
| NM_178156.2:c.-228+59145_-228+59146insAGATC (FUT8) | NP_835369.1:n.-228+59145_-228+59146insAGATC | |
| NR_030355.1:n.37_38insAGATC (MIR625) | ||
| NR_038167.1:n.1500+15420_1500+15421insAGATC (FUT8) | ||
| NR_038170.1:n.583+15420_583+15421insAGATC (FUT8) | ||
| XM_011536613.1:c.-228+57924_-228+57925insAGATC (FUT8) | XP_011534915.1:n.-228+57924_-228+57925insAGATC | |
| XM_017021136.1:c.-228+15420_-228+15421insAGATC (FUT8) | XP_016876625.1:n.-228+15420_-228+15421insAGATC | |
| XM_017021137.1:c.-228+15420_-228+15421insAGATC (FUT8) | XP_016876626.1:n.-228+15420_-228+15421insAGATC | |
| XM_017021138.1:c.-228+59145_-228+59146insAGATC (FUT8) | XP_016876627.1:n.-228+59145_-228+59146insAGATC | |
| XM_017021139.1:c.-228+57924_-228+57925insAGATC (FUT8) | XP_016876628.1:n.-228+57924_-228+57925insAGATC | |
| NM_001371533.1:c.-228+15420_-228+15421insAGATC (FUT8) MANE Select | NP_001358462.1:n.-228+15420_-228+15421insAGATC | |
| NM_001371534.1:c.-228+15420_-228+15421insAGATC (FUT8) | NP_001358463.1:n.-228+15420_-228+15421insAGATC | |
| NM_001371536.1:c.-228+15420_-228+15421insAGATC (FUT8) | NP_001358465.1:n.-228+15420_-228+15421insAGATC | |
| NM_178155.3:c.-228+15420_-228+15421insAGATC (FUT8) | NP_835368.1:n.-228+15420_-228+15421insAGATC |