Linked Data
dbSNP Id:
rs797044894
MyVariant Identifiers:
chr10:g.76788683_76788684insGAAGAAGAA (hg19)
chr10:g.75028925_75028926insGAAGAAGAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.75028929_75028930insAAGAAGAAG , CM000672.2:g.75028929_75028930insAAGAAGAAG | GRCh38 |
| NC_000010.10:g.76788687_76788688insAAGAAGAAG , CM000672.1:g.76788687_76788688insAAGAAGAAG | GRCh37 |
| NC_000010.9:g.76458693_76458694insAAGAAGAAG | NCBI36 |
| NG_032048.1:g.207517_207518insAAGAAGAAG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000287239.10:c.4105_4106insAAGAAGAAG (KAT6B) MANE Select | ENSP00000287239.4:p.Glu1368_Gly1369insGlu... | |
| ENST00000372711.2:c.3556_3557insAAGAAGAAG (KAT6B) | ENSP00000361796.1:p.Glu1185_Gly1186insGlu... | |
| ENST00000372714.6:c.3229_3230insAAGAAGAAG (KAT6B) | ENSP00000361799.1:p.Glu1076_Gly1077insGlu... | |
| ENST00000372724.6:c.3556_3557insAAGAAGAAG (KAT6B) | ENSP00000361809.2:p.Glu1185_Gly1186insGlu... | |
| ENST00000372725.6:c.3229_3230insAAGAAGAAG (KAT6B) | ENSP00000361810.1:p.Glu1076_Gly1077insGlu... | |
| ENST00000648048.1:c.4105_4106insAAGAAGAAG (KAT6B) | ENSP00000497325.1:p.Glu1368_Gly1369insGlu... | |
| ENST00000648725.1:c.4105_4106insAAGAAGAAG (KAT6B) | ENSP00000497841.1:p.Glu1368_Gly1369insGlu... | |
| ENST00000648892.1:c.3229_3230insAAGAAGAAG (KAT6B) | ENSP00000497048.1:p.Glu1076_Gly1077insGlu... | |
| ENST00000649006.1:c.3229_3230insAAGAAGAAG (KAT6B) | ENSP00000498139.1:p.Glu1076_Gly1077insGlu... | |
| ENST00000649463.1:c.4105_4106insAAGAAGAAG (KAT6B) | ENSP00000497166.1:p.Glu1368_Gly1369insGlu... | |
| ENST00000287239.8:c.4105_4106insAAGAAGAAG (KAT6B) | ENSP00000287239.4:p.Glu1368_Gly1369insGlu... | |
| ENST00000372711.1:c.3556_3557insAAGAAGAAG (KAT6B) | ENSP00000361796.1:p.Glu1185_Gly1186insGlu... | |
| ENST00000372714.5:c.3229_3230insAAGAAGAAG (KAT6B) | ENSP00000361799.1:p.Glu1076_Gly1077insGlu... | |
| ENST00000372724.5:c.3229_3230insAAGAAGAAG (KAT6B) | ENSP00000361809.1:p.Glu1076_Gly1077insGlu... | |
| ENST00000372725.5:c.3229_3230insAAGAAGAAG (KAT6B) | ENSP00000361810.1:p.Glu1076_Gly1077insGlu... | |
| NM_001256468.1:c.3556_3557insAAGAAGAAG (KAT6B) | NP_001243397.1:p.Glu1185_Gly1186insGluGlu... | |
| NM_001256469.1:c.3229_3230insAAGAAGAAG (KAT6B) | NP_001243398.1:p.Glu1076_Gly1077insGluGlu... | |
| NM_012330.3:c.4105_4106insAAGAAGAAG (KAT6B) | NP_036462.2:p.Glu1368_Gly1369insGluGluGlu... | |
| XM_005269664.2:c.4105_4106insAAGAAGAAG (KAT6B) | XP_005269721.1:p.Glu1368_Gly1369insGluGlu... | |
| XR_946064.1:n.577-2332_577-2331insTTCTTCTTC | ||
| XM_011539747.2:c.*3622-2332_*3622-2331insTTCTTCTTC (DUSP29) | XP_011538049.1:n.*3622-2332_*3622-2331ins... | |
| XM_017016000.2:c.4105_4106insAAGAAGAAG (KAT6B) | XP_016871489.1:p.Glu1368_Gly1369insGluGlu... | |
| XM_017016002.1:c.4105_4106insAAGAAGAAG (KAT6B) | XP_016871491.1:p.Glu1368_Gly1369insGluGlu... | |
| XM_017016003.1:c.4105_4106insAAGAAGAAG (KAT6B) | XP_016871492.1:p.Glu1368_Gly1369insGluGlu... | |
| XM_017016004.2:c.3943_3944insAAGAAGAAG (KAT6B) | XP_016871493.1:p.Glu1314_Gly1315insGluGlu... | |
| XM_017016005.2:c.3556_3557insAAGAAGAAG (KAT6B) | XP_016871494.1:p.Glu1185_Gly1186insGluGlu... | |
| XM_017016006.2:c.3229_3230insAAGAAGAAG (KAT6B) | XP_016871495.1:p.Glu1076_Gly1077insGluGlu... | |
| XM_017016008.2:c.3229_3230insAAGAAGAAG (KAT6B) | XP_016871497.1:p.Glu1076_Gly1077insGluGlu... | |
| XM_017016009.1:c.3067_3068insAAGAAGAAG (KAT6B) | XP_016871498.1:p.Glu1022_Gly1023insGluGlu... | |
| NM_012330.4:c.4105_4106insAAGAAGAAG (KAT6B) MANE Select | NP_036462.2:p.Glu1368_Gly1369insGluGluGlu... | |
| NM_001370132.1:c.3067_3068insAAGAAGAAG (KAT6B) | NP_001357061.1:p.Glu1022_Gly1023insGluGlu... | |
| NM_001370133.1:c.2416_2417insAAGAAGAAG (KAT6B) | NP_001357062.1:p.Glu805_Gly806insGluGluGl... | |
| NM_001370134.1:c.2020_2021insAAGAAGAAG (KAT6B) | NP_001357063.1:p.Glu673_Gly674insGluGluGl... | |
| NM_001370135.1:c.1762_1763insAAGAAGAAG (KAT6B) | NP_001357064.1:p.Glu587_Gly588insGluGluGl... | |
| NM_001370136.1:c.4105_4106insAAGAAGAAG (KAT6B) | NP_001357065.1:p.Glu1368_Gly1369insGluGlu... | |
| NM_001370137.1:c.4105_4106insAAGAAGAAG (KAT6B) | NP_001357066.1:p.Glu1368_Gly1369insGluGlu... | |
| NM_001370138.1:c.3556_3557insAAGAAGAAG (KAT6B) | NP_001357067.1:p.Glu1185_Gly1186insGluGlu... | |
| NM_001370139.1:c.3229_3230insAAGAAGAAG (KAT6B) | NP_001357068.1:p.Glu1076_Gly1077insGluGlu... | |
| NM_001370140.1:c.3229_3230insAAGAAGAAG (KAT6B) | NP_001357069.1:p.Glu1076_Gly1077insGluGlu... | |
| NM_001370141.1:c.3229_3230insAAGAAGAAG (KAT6B) | NP_001357070.1:p.Glu1076_Gly1077insGluGlu... | |
| NM_001370142.1:c.3229_3230insAAGAAGAAG (KAT6B) | NP_001357071.1:p.Glu1076_Gly1077insGluGlu... | |
| NM_001370143.1:c.3040_3041insAAGAAGAAG (KAT6B) | NP_001357072.1:p.Glu1013_Gly1014insGluGlu... | |
| NM_001370144.1:c.3040_3041insAAGAAGAAG (KAT6B) | NP_001357073.1:p.Glu1013_Gly1014insGluGlu... | |
| NM_001256468.2:c.3556_3557insAAGAAGAAG (KAT6B) | NP_001243397.1:p.Glu1185_Gly1186insGluGlu... | |
| NM_001256469.2:c.3229_3230insAAGAAGAAG (KAT6B) | NP_001243398.1:p.Glu1076_Gly1077insGluGlu... |