Linked Data
MyVariant Identifiers:
chr14:g.23889446_23889447insC (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23420237_23420238insC , CM000676.2:g.23420237_23420238insC | GRCh38 |
| NC_000014.8:g.23889446_23889447insC , CM000676.1:g.23889446_23889447insC | GRCh37 |
| NC_000014.7:g.22959286_22959287insC | NCBI36 |
| NG_007884.1:g.20424_20425insG , LRG_384:g.20424_20425insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3337-4_3337-3insG MANE Select | ENSP00000347507.3:n.3337-4_3337-3insG | |
| ENST00000355349.3:c.3337-4_3337-3insG | ENSP00000347507.3:n.3337-4_3337-3insG | |
| NM_000257.3:c.3337-4_3337-3insG | NP_000248.2:n.3337-4_3337-3insG | |
| XR_245686.3:n.3445-4_3445-3insG | ||
| XM_017021340.1:c.3337-4_3337-3insG | XP_016876829.1:n.3337-4_3337-3insG | |
| NM_000257.4:c.3337-4_3337-3insG MANE Select | NP_000248.2:n.3337-4_3337-3insG |