Linked Data
MyVariant Identifiers:
chr1:g.186649430_186649436del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680299_186680305del , CM000663.2:g.186680299_186680305del | GRCh38 |
| NC_000001.10:g.186649431_186649437del , CM000663.1:g.186649431_186649437del | GRCh37 |
| NC_000001.9:g.184916054_184916060del | NCBI36 |
| NG_028206.2:g.5124_5130del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367468.10:c.-14_-8del MANE Select | ENSP00000356438.5:n.-14_-8del | |
| ENST00000680451.1:c.-14_-8del | ENSP00000506242.1:n.-14_-8del | |
| ENST00000681605.1:c.-14_-8del | ENSP00000504900.1:n.-14_-8del | |
| ENST00000367468.9:c.-14_-8del | ENSP00000356438.5:n.-14_-8del | |
| ENST00000490885.6:n.120_126del | ||
| ENST00000559800.1:n.120_126del | ||
| NM_000963.3:c.-14_-8del | NP_000954.1:n.-14_-8del | |
| NM_000963.4:c.-14_-8del MANE Select | NP_000954.1:n.-14_-8del |