Linked Data
dbSNP Id:
rs1564368361
gnomAD v2:
9-140061821-C-CGT
gnomAD v4:
9-137167369-C-CGT
MyVariant Identifiers:
chr9:g.140061821_140061822insGT (hg19)
chr9:g.137167369_137167370insGT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137167370_137167371insTG , CM000671.2:g.137167370_137167371insTG | GRCh38 |
| NC_000009.11:g.140061822_140061823insTG , CM000671.1:g.140061822_140061823insTG | GRCh37 |
| NC_000009.10:g.139181643_139181644insTG | NCBI36 |
| NG_011507.1:g.33214_33215insTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371553.8:c.2764-404_2764-403insTG | ENSP00000360608.3:n.2764-404_2764-403insTG | |
| ENST00000371560.5:c.2653-404_2653-403insTG | ENSP00000360615.3:n.2653-404_2653-403insTG | |
| ENST00000371561.8:c.2701-41_2701-40insTG MANE Select | ENSP00000360616.3:n.2701-41_2701-40insTG | |
| ENST00000371546.8:c.2764-41_2764-40insTG | ENSP00000360601.4:n.2764-41_2764-40insTG | |
| ENST00000371550.8:c.2590-41_2590-40insTG | ENSP00000360605.4:n.2590-41_2590-40insTG | |
| ENST00000371553.7:c.2764-404_2764-403insTG | ENSP00000360608.3:n.2764-404_2764-403insTG | |
| ENST00000371555.8:c.2653-41_2653-40insTG | ENSP00000360610.4:n.2653-41_2653-40insTG | |
| ENST00000371559.8:c.2590-404_2590-403insTG | ENSP00000360614.4:n.2590-404_2590-403insTG | |
| ENST00000371560.4:c.2653-404_2653-403insTG | ENSP00000360615.3:n.2653-404_2653-403insTG | |
| ENST00000371561.7:c.2701-41_2701-40insTG | ENSP00000360616.3:n.2701-41_2701-40insTG | |
| ENST00000473811.1:n.181-41_181-40insTG | ||
| NM_000832.6:c.2590-404_2590-403insTG | NP_000823.4:n.2590-404_2590-403insTG | |
| NM_001185090.1:c.2764-404_2764-403insTG | NP_001172019.1:n.2764-404_2764-403insTG | |
| NM_001185091.1:c.2653-404_2653-403insTG | NP_001172020.1:n.2653-404_2653-403insTG | |
| NM_007327.3:c.2701-41_2701-40insTG | NP_015566.1:n.2701-41_2701-40insTG | |
| NM_021569.3:c.2590-41_2590-40insTG | NP_067544.1:n.2590-41_2590-40insTG | |
| XM_005266071.2:c.2701-404_2701-403insTG | XP_005266128.1:n.2701-404_2701-403insTG | |
| XM_005266072.2:c.2653-41_2653-40insTG | XP_005266129.1:n.2653-41_2653-40insTG | |
| XM_005266073.3:c.2764-41_2764-40insTG | XP_005266130.1:n.2764-41_2764-40insTG | |
| XM_005266071.3:c.2701-404_2701-403insTG | XP_005266128.1:n.2701-404_2701-403insTG | |
| XM_005266072.3:c.2653-41_2653-40insTG | XP_005266129.1:n.2653-41_2653-40insTG | |
| XM_005266073.4:c.2764-41_2764-40insTG | XP_005266130.1:n.2764-41_2764-40insTG | |
| NM_007327.4:c.2701-41_2701-40insTG MANE Select | NP_015566.1:n.2701-41_2701-40insTG | |
| NM_000832.7:c.2590-404_2590-403insTG | NP_000823.4:n.2590-404_2590-403insTG | |
| NM_001185090.2:c.2764-404_2764-403insTG | NP_001172019.1:n.2764-404_2764-403insTG | |
| NM_001185091.2:c.2653-404_2653-403insTG | NP_001172020.1:n.2653-404_2653-403insTG | |
| NM_021569.4:c.2590-41_2590-40insTG | NP_067544.1:n.2590-41_2590-40insTG |