ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.36976197_36976198delinsCC , CM000667.2:g.36976197_36976198delinsCC | GRCh38 |
| NC_000005.9:g.36976299_36976300delinsCC , CM000667.1:g.36976299_36976300delinsCC | GRCh37 |
| NC_000005.8:g.37012056_37012057delinsCC | NCBI36 |
| NG_006987.1:g.104315_104316delinsCC | |
| NG_006987.2:g.104315_104316delinsCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282516.13:c.1290_1291delinsCC MANE Select | ENSP00000282516.8:p.Ala431Pro | |
| ENST00000652901.1:c.1290_1291delinsCC | ENSP00000499536.1:p.Ala431Pro | |
| ENST00000282516.12:c.1290_1291delinsCC | ENSP00000282516.8:p.Ala431Pro | |
| ENST00000448238.2:c.1290_1291delinsCC | ENSP00000406266.2:p.Ala431Pro | |
| ENST00000504430.5:n.910_911delinsCC | ||
| ENST00000621733.1:c.1-88381_1-88380delinsCC | ENSP00000480694.1:n.1-88381_1-88380delinsCC | |
| NM_015384.4:c.1290_1291delinsCC | NP_056199.2:p.Ala431Pro | |
| NM_133433.3:c.1290_1291delinsCC | NP_597677.2:p.Ala431Pro | |
| XM_005248280.2:c.1290_1291delinsCC | XP_005248337.1:p.Ala431Pro | |
| XM_005248282.3:c.546_547delinsCC | XP_005248339.2:p.Ala183Pro | |
| XM_006714467.2:c.1290_1291delinsCC | XP_006714530.1:p.Ala431Pro | |
| XM_006714468.1:c.1290_1291delinsCC | XP_006714531.1:p.Ala431Pro | |
| XM_011514014.1:c.1290_1291delinsCC | XP_011512316.1:p.Ala431Pro | |
| XM_011514015.1:c.1290_1291delinsCC | XP_011512317.1:p.Ala431Pro | |
| XM_005248280.3:c.1290_1291delinsCC | XP_005248337.1:p.Ala431Pro | |
| XM_005248282.5:c.630_631delinsCC | XP_005248339.3:p.Ala211Pro | |
| XM_006714468.2:c.1290_1291delinsCC | XP_006714531.1:p.Ala431Pro | |
| XM_017009329.1:c.1290_1291delinsCC | XP_016864818.1:p.Ala431Pro | |
| XM_017009331.1:c.1290_1291delinsCC | XP_016864820.1:p.Ala431Pro | |
| NM_133433.4:c.1290_1291delinsCC MANE Select | NP_597677.2:p.Ala431Pro | |
| NM_015384.5:c.1290_1291delinsCC | NP_056199.2:p.Ala431Pro |