Linked Data
dbSNP Id:
rs1162070167
gnomAD v2:
3-93593274-T-TTTTG
MyVariant Identifiers:
chr3:g.93593274_93593275insTTTG (hg19)
chr3:g.93874430_93874431insTTTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.93874431_93874432insTTGT , CM000665.2:g.93874431_93874432insTTGT | GRCh38 |
| NC_000003.11:g.93593275_93593276insTTGT , CM000665.1:g.93593275_93593276insTTGT | GRCh37 |
| NC_000003.10:g.95075965_95075966insTTGT | NCBI36 |
| NG_009813.1:g.104660_104661insCAAA , LRG_572:g.104660_104661insCAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000348974.5:c.1871-26_1871-25insCAAA | ENSP00000330021.7:n.1871-26_1871-25insCAAA | |
| ENST00000394236.9:c.1871-26_1871-25insCAAA MANE Select | ENSP00000377783.3:n.1871-26_1871-25insCAAA | |
| ENST00000407433.6:c.1826-26_1826-25insCAAA | ENSP00000385794.2:n.1826-26_1826-25insCAAA | |
| ENST00000647936.1:c.1645-26_1645-25insCAAA | ENSP00000496822.1:n.1645-26_1645-25insCAAA | |
| ENST00000648381.1:n.2039-26_2039-25insCAAA | ||
| ENST00000648853.1:c.1829-26_1829-25insCAAA | ENSP00000497262.1:n.1829-26_1829-25insCAAA | |
| ENST00000650591.1:c.1967-26_1967-25insCAAA | ENSP00000497376.1:n.1967-26_1967-25insCAAA | |
| ENST00000394236.7:c.1871-26_1871-25insCAAA | ENSP00000377783.3:n.1871-26_1871-25insCAAA | |
| ENST00000407433.5:c.1478-26_1478-25insCAAA | ENSP00000385794.1:n.1478-26_1478-25insCAAA | |
| NM_000313.3:c.1871-26_1871-25insCAAA , LRG_572t1:c.1871-26_1871-25insCAAA | NP_000304.2:n.1871-26_1871-25insCAAA | |
| NM_001314077.1:c.1967-26_1967-25insCAAA , LRG_572t2:c.1967-26_1967-25insCAAA | NP_001301006.1:n.1967-26_1967-25insCAAA | |
| NM_000313.4:c.1871-26_1871-25insCAAA MANE Select | NP_000304.2:n.1871-26_1871-25insCAAA | |
| NM_001314077.2:c.1967-26_1967-25insCAAA | NP_001301006.1:n.1967-26_1967-25insCAAA |