Linked Data
dbSNP Id:
rs1199324026
MyVariant Identifiers:
chr6:g.20661041_20661042insATTG (hg19)
chr6:g.20660810_20660811insATTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.20660811_20660814dup , CM000668.2:g.20660811_20660814dup | GRCh38 |
| NC_000006.11:g.20661042_20661045dup , CM000668.1:g.20661042_20661045dup | GRCh37 |
| NC_000006.10:g.20769021_20769024dup | NCBI36 |
| NG_021195.1:g.131355_131358dup | |
| NG_021195.2:g.131355_131358dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000274695.8:c.371+11434_371+11437dup MANE Select | ENSP00000274695.4:n.371+11434_371+11437du... | |
| ENST00000378610.1:c.371+11434_371+11437dup | ENSP00000367873.1:n.371+11434_371+11437du... | |
| NM_017774.3:c.371+11434_371+11437dup MANE Select | NP_060244.2:n.371+11434_371+11437dup | |
| XM_006715128.2:c.371+11434_371+11437dup | XP_006715191.1:n.371+11434_371+11437dup | |
| XM_011514718.1:c.371+11434_371+11437dup | XP_011513020.1:n.371+11434_371+11437dup | |
| XM_011514719.1:c.371+11434_371+11437dup | XP_011513021.1:n.371+11434_371+11437dup | |
| XR_926265.1:n.538+11434_538+11437dup | ||
| XR_926266.1:n.651+11434_651+11437dup | ||
| XR_926267.1:n.538+11434_538+11437dup | ||
| XM_011514719.2:c.371+11434_371+11437dup | XP_011513021.1:n.371+11434_371+11437dup | |
| XM_017010986.1:c.371+11434_371+11437dup | XP_016866475.1:n.371+11434_371+11437dup | |
| XM_017010987.1:c.-384+11434_-384+11437dup | XP_016866476.1:n.-384+11434_-384+11437dup... | |
| XM_024446481.1:c.371+11434_371+11437dup | XP_024302249.1:n.371+11434_371+11437dup | |
| XR_001743495.2:n.543+11434_543+11437dup | ||
| XR_001743496.2:n.938+11434_938+11437dup | ||
| XR_001743500.1:n.538+11434_538+11437dup | ||
| XR_001743501.1:n.538+11434_538+11437dup | ||
| XR_926265.2:n.538+11434_538+11437dup | ||
| XR_926266.2:n.651+11434_651+11437dup | ||
| XR_926267.2:n.538+11434_538+11437dup |