Linked Data
dbSNP Id:
rs1184720975
gnomAD v2:
2-149216489-A-ATAT
MyVariant Identifiers:
chr2:g.149216489_149216490insTAT (hg19)
chr2:g.148458920_148458921insTAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.148458920_148458921insTAT , CM000664.2:g.148458920_148458921insTAT | GRCh38 |
| NC_000002.11:g.149216489_149216490insTAT , CM000664.1:g.149216489_149216490insTAT | GRCh37 |
| NC_000002.10:g.148932959_148932960insTAT | NCBI36 |
| NG_017003.1:g.442910_442911insTAT | |
| NG_017003.2:g.442910_442911insTAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000637159.1:c.113+49_113+50insTAT | ENSP00000490140.1:n.113+49_113+50insTAT | |
| ENST00000638043.2:c.113+49_113+50insTAT | ENSP00000490728.2:n.113+49_113+50insTAT | |
| ENST00000642680.2:c.113+49_113+50insTAT MANE Select | ENSP00000493871.2:n.113+49_113+50insTAT | |
| ENST00000404807.5:c.113+49_113+50insTAT | ENSP00000384672.1:n.113+49_113+50insTAT | |
| ENST00000407073.5:c.113+49_113+50insTAT | ENSP00000386049.1:n.113+49_113+50insTAT | |
| ENST00000627651.2:c.113+49_113+50insTAT | ENSP00000486370.1:n.113+49_113+50insTAT | |
| ENST00000629878.2:c.113+49_113+50insTAT | ENSP00000487089.1:n.113+49_113+50insTAT | |
| NM_018328.4:c.113+49_113+50insTAT | NP_060798.2:n.113+49_113+50insTAT | |
| XM_005263711.2:c.113+49_113+50insTAT | XP_005263768.1:n.113+49_113+50insTAT | |
| XM_011511470.1:c.113+49_113+50insTAT | XP_011509772.1:n.113+49_113+50insTAT | |
| XM_011511471.1:c.113+49_113+50insTAT | XP_011509773.1:n.113+49_113+50insTAT | |
| XM_011511472.1:c.113+49_113+50insTAT | XP_011509774.1:n.113+49_113+50insTAT | |
| XM_011511473.1:c.113+49_113+50insTAT | XP_011509775.1:n.113+49_113+50insTAT | |
| XM_011511474.1:c.113+49_113+50insTAT | XP_011509776.1:n.113+49_113+50insTAT | |
| XM_011511475.1:c.113+49_113+50insTAT | XP_011509777.1:n.113+49_113+50insTAT | |
| XM_011511476.1:c.113+49_113+50insTAT | XP_011509778.1:n.113+49_113+50insTAT | |
| XR_922967.1:n.1342+49_1342+50insTAT | ||
| XM_011511470.2:c.113+49_113+50insTAT | XP_011509772.1:n.113+49_113+50insTAT | |
| XM_011511472.2:c.113+49_113+50insTAT | XP_011509774.1:n.113+49_113+50insTAT | |
| XM_024452987.1:c.113+49_113+50insTAT | XP_024308755.1:n.113+49_113+50insTAT | |
| XM_024452988.1:c.113+49_113+50insTAT | XP_024308756.1:n.113+49_113+50insTAT | |
| XM_024452989.1:c.113+49_113+50insTAT | XP_024308757.1:n.113+49_113+50insTAT | |
| XM_024452990.1:c.113+49_113+50insTAT | XP_024308758.1:n.113+49_113+50insTAT | |
| XR_002959318.1:n.425+49_425+50insTAT | ||
| XR_002959319.1:n.425+49_425+50insTAT | ||
| NM_001378120.1:c.113+49_113+50insTAT MANE Select | NP_001365049.1:n.113+49_113+50insTAT | |
| NM_018328.5:c.113+49_113+50insTAT | NP_060798.2:n.113+49_113+50insTAT |