Revel Score:
ENST00000282516 (MANE Select)
0.740
ENST00000448238
0.740
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.36953700A>C , CM000667.2:g.36953700A>C | GRCh38 |
| NC_000005.9:g.36953802A>C , CM000667.1:g.36953802A>C | GRCh37 |
| NC_000005.8:g.36989559A>C | NCBI36 |
| NG_006987.1:g.81818A>C | |
| NG_006987.2:g.81818A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282516.13:c.4A>C MANE Select | ENSP00000282516.8:p.Asn2His | |
| ENST00000652901.1:c.4A>C | ENSP00000499536.1:p.Asn2His | |
| ENST00000282516.12:c.4A>C | ENSP00000282516.8:p.Asn2His | |
| ENST00000448238.2:c.4A>C | ENSP00000406266.2:p.Asn2His | |
| ENST00000621733.1:c.-1+76678A>C | ENSP00000480694.1:n.-1+76678A>C | |
| NM_015384.4:c.4A>C | NP_056199.2:p.Asn2His | |
| NM_133433.3:c.4A>C | NP_597677.2:p.Asn2His | |
| XM_005248280.2:c.4A>C | XP_005248337.1:p.Asn2His | |
| XM_006714467.2:c.4A>C | XP_006714530.1:p.Asn2His | |
| XM_006714468.1:c.4A>C | XP_006714531.1:p.Asn2His | |
| XM_011514014.1:c.4A>C | XP_011512316.1:p.Asn2His | |
| XM_011514015.1:c.4A>C | XP_011512317.1:p.Asn2His | |
| XM_005248280.3:c.4A>C | XP_005248337.1:p.Asn2His | |
| XM_006714468.2:c.4A>C | XP_006714531.1:p.Asn2His | |
| XM_017009329.1:c.4A>C | XP_016864818.1:p.Asn2His | |
| XM_017009331.1:c.4A>C | XP_016864820.1:p.Asn2His | |
| NM_133433.4:c.4A>C MANE Select | NP_597677.2:p.Asn2His | |
| NM_015384.5:c.4A>C | NP_056199.2:p.Asn2His |