Linked Data
dbSNP Id:
rs1420118365
gnomAD v3:
9-96298647-T-TGGTG
gnomAD v4:
9-96298647-T-TGGTG
MyVariant Identifiers:
chr9:g.99060929_99060930insGGTG (hg19)
chr9:g.96298647_96298648insGGTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.96298655_96298658dup , CM000671.2:g.96298655_96298658dup | GRCh38 |
| NC_000009.11:g.99060937_99060940dup , CM000671.1:g.99060937_99060940dup | GRCh37 |
| NC_000009.10:g.98100758_98100761dup | NCBI36 |
| NG_008157.1:g.8502_8505dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375262.4:c.155-189_155-186dup | ENSP00000364411.2:n.155-189_155-186dup | |
| ENST00000375263.8:c.155-189_155-186dup MANE Select | ENSP00000364412.3:n.155-189_155-186dup | |
| ENST00000463517.2:n.964-189_964-186dup | ||
| ENST00000464104.6:n.625-189_625-186dup | ||
| ENST00000467499.6:c.155-189_155-186dup | ENSP00000498077.1:n.155-189_155-186dup | |
| ENST00000643789.1:c.2447-189_2447-186dup | ||
| ENST00000648146.1:c.155-189_155-186dup | ENSP00000497238.1:n.155-189_155-186dup | |
| ENST00000648332.1:c.155-189_155-186dup | ENSP00000497562.1:n.155-189_155-186dup | |
| ENST00000648799.1:c.155-189_155-186dup | ENSP00000498039.1:n.155-189_155-186dup | |
| ENST00000650005.1:c.155-189_155-186dup | ENSP00000498121.1:n.155-189_155-186dup | |
| ENST00000650386.1:c.155-189_155-186dup | ENSP00000497464.1:n.155-189_155-186dup | |
| ENST00000375262.3:c.155-189_155-186dup | ENSP00000364411.2:n.155-189_155-186dup | |
| ENST00000375263.7:c.155-189_155-186dup | ENSP00000364412.3:n.155-189_155-186dup | |
| NM_000197.1:c.155-189_155-186dup | NP_000188.1:n.155-189_155-186dup | |
| XM_006717095.2:c.155-189_155-186dup | XP_006717158.1:n.155-189_155-186dup | |
| XM_011518618.1:c.155-189_155-186dup | XP_011516920.1:n.155-189_155-186dup | |
| XM_011518619.1:c.155-189_155-186dup | XP_011516921.1:n.155-189_155-186dup | |
| XM_011518620.1:c.155-189_155-186dup | XP_011516922.1:n.155-189_155-186dup | |
| XM_011518621.1:c.155-189_155-186dup | XP_011516923.1:n.155-189_155-186dup | |
| NM_000197.2:c.155-189_155-186dup MANE Select | NP_000188.1:n.155-189_155-186dup | |
| XM_011518618.2:c.155-189_155-186dup | XP_011516920.1:n.155-189_155-186dup | |
| XM_011518619.2:c.155-189_155-186dup | XP_011516921.1:n.155-189_155-186dup | |
| XM_017014671.1:c.155-189_155-186dup | XP_016870160.1:n.155-189_155-186dup | |
| XM_017014672.1:c.155-189_155-186dup | XP_016870161.1:n.155-189_155-186dup | |
| XM_017014673.2:c.155-189_155-186dup | XP_016870162.1:n.155-189_155-186dup | |
| XM_017014674.1:c.155-189_155-186dup | XP_016870163.1:n.155-189_155-186dup | |
| XM_017014675.1:c.69-189_69-186dup | XP_016870164.1:n.69-189_69-186dup | |
| XM_017014677.1:c.-782-189_-782-186dup | XP_016870166.1:n.-782-189_-782-186dup | |
| XM_024447529.1:c.69-189_69-186dup | XP_024303297.1:n.69-189_69-186dup | |
| XR_002956778.1:n.2589-189_2589-186dup |