Linked Data
dbSNP Id:
rs1285160561
gnomAD v2:
3-38950942-T-TCAAGA
gnomAD v3:
3-38909451-T-TCAAGA
gnomAD v4:
3-38909451-T-TCAAGA
MyVariant Identifiers:
chr3:g.38950942_38950943insCAAGA (hg19)
chr3:g.38909451_38909452insCAAGA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38909451_38909452insCAAGA , CM000665.2:g.38909451_38909452insCAAGA | GRCh38 |
| NC_000003.11:g.38950942_38950943insCAAGA , CM000665.1:g.38950942_38950943insCAAGA | GRCh37 |
| NC_000003.10:g.38925946_38925947insCAAGA | NCBI36 |
| NG_033859.1:g.46110_46111insTCTTG | |
| NG_033859.2:g.147535_147536insTCTTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302328.9:c.1102-258_1102-257insTCTTG MANE Select | ENSP00000307599.3:n.1102-258_1102-257insTCTTG | |
| ENST00000668754.1:c.1102-258_1102-257insTCTTG | ENSP00000499569.1:n.1102-258_1102-257insTCTTG | |
| ENST00000675223.1:c.1102-258_1102-257insTCTTG | ENSP00000502481.1:n.1102-258_1102-257insTCTTG | |
| ENST00000675672.1:c.1102-258_1102-257insTCTTG | ENSP00000502446.1:n.1102-258_1102-257insTCTTG | |
| ENST00000675892.1:c.922-258_922-257insTCTTG | ENSP00000502318.1:n.922-258_922-257insTCTTG | |
| ENST00000676045.1:c.1146-258_1146-257insTCTTG | ENSP00000501685.1:n.1146-258_1146-257insTCTTG | |
| ENST00000676176.1:c.1102-258_1102-257insTCTTG | ENSP00000501891.1:n.1102-258_1102-257insTCTTG | |
| ENST00000302328.7:c.1102-258_1102-257insTCTTG | ENSP00000307599.3:n.1102-258_1102-257insTCTTG | |
| ENST00000444237.2:c.1102-258_1102-257insTCTTG | ENSP00000408028.2:n.1102-258_1102-257insTCTTG | |
| ENST00000456224.7:c.1102-258_1102-257insTCTTG | ENSP00000416757.3:n.1102-258_1102-257insTCTTG | |
| NM_001287223.1:c.1102-258_1102-257insTCTTG | NP_001274152.1:n.1102-258_1102-257insTCTTG | |
| NM_014139.2:c.1102-258_1102-257insTCTTG | NP_054858.2:n.1102-258_1102-257insTCTTG | |
| XM_011533320.1:c.1102-258_1102-257insTCTTG | XP_011531622.1:n.1102-258_1102-257insTCTTG | |
| XM_011533321.1:c.439-258_439-257insTCTTG | XP_011531623.1:n.439-258_439-257insTCTTG | |
| NM_001349253.1:c.1102-258_1102-257insTCTTG | NP_001336182.1:n.1102-258_1102-257insTCTTG | |
| XM_011533321.2:c.439-258_439-257insTCTTG | XP_011531623.1:n.439-258_439-257insTCTTG | |
| XM_017005647.1:c.1477-258_1477-257insTCTTG | XP_016861136.1:n.1477-258_1477-257insTCTTG | |
| XM_017005648.1:c.1101+614_1101+615insTCTTG | XP_016861137.1:n.1101+614_1101+615insTCTTG | |
| XM_017005650.1:c.1102-258_1102-257insTCTTG | XP_016861139.1:n.1102-258_1102-257insTCTTG | |
| XM_017005651.1:c.829-258_829-257insTCTTG | XP_016861140.1:n.829-258_829-257insTCTTG | |
| XM_017005652.1:c.1102-258_1102-257insTCTTG | XP_016861141.1:n.1102-258_1102-257insTCTTG | |
| NM_001349253.2:c.1102-258_1102-257insTCTTG MANE Select | NP_001336182.1:n.1102-258_1102-257insTCTTG | |
| NM_014139.3:c.1102-258_1102-257insTCTTG | NP_054858.2:n.1102-258_1102-257insTCTTG |