Linked Data
dbSNP Id:
rs777094270
MyVariant Identifiers:
chr4:g.178361818_178361819insTC (hg19)
chr4:g.177440664_177440665insTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177440664_177440665insTC , CM000666.2:g.177440664_177440665insTC | GRCh38 |
| NC_000004.11:g.178361818_178361819insTC , CM000666.1:g.178361818_178361819insTC | GRCh37 |
| NC_000004.10:g.178598812_178598813insTC | NCBI36 |
| NG_011845.2:g.6839_6840insGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264595.7:c.128-239_128-238insGA MANE Select | ENSP00000264595.2:n.128-239_128-238insGA | |
| ENST00000264595.6:c.128-239_128-238insGA | ENSP00000264595.2:n.128-239_128-238insGA | |
| ENST00000506853.5:n.162-239_162-238insGA | ||
| ENST00000510955.5:n.162-239_162-238insGA | ||
| ENST00000511231.1:n.162-239_162-238insGA | ||
| NM_000027.3:c.128-239_128-238insGA | NP_000018.2:n.128-239_128-238insGA | |
| NM_001171988.1:c.128-239_128-238insGA | NP_001165459.1:n.128-239_128-238insGA | |
| NR_033655.1:n.256-239_256-238insGA | ||
| XM_006714123.2:c.128-239_128-238insGA | XP_006714186.1:n.128-239_128-238insGA | |
| XR_001741155.2:n.222-239_222-238insGA | ||
| NM_000027.4:c.128-239_128-238insGA MANE Select | NP_000018.2:n.128-239_128-238insGA | |
| NM_001171988.2:c.128-239_128-238insGA | NP_001165459.1:n.128-239_128-238insGA | |
| NR_033655.2:n.190-239_190-238insGA |