Linked Data
ClinVar Variation Id:
371193
ClinVar RCV Id:
RCV001580492
dbSNP Id:
rs1057517078
gnomAD v4:
6-51867882-GA-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51867887del , CM000668.2:g.51867887del | GRCh38 |
| NC_000006.11:g.51732685del , CM000668.1:g.51732685del | GRCh37 |
| NC_000006.10:g.51840644del | NCBI36 |
| NG_008753.1:g.224743del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371117.8:c.7713del MANE Select | ENSP00000360158.3:p.His2572IlefsTer7 | |
| ENST00000340994.4:c.7713del | ENSP00000341097.4:p.His2572IlefsTer7 | |
| ENST00000371117.7:c.7713del | ENSP00000360158.3:p.His2572IlefsTer7 | |
| NM_138694.3:c.7713del | NP_619639.3:p.His2572IlefsTer7 | |
| NM_170724.2:c.7713del | NP_733842.2:p.His2572IlefsTer7 | |
| XM_011514679.1:c.7713del | XP_011512981.1:p.His2572IlefsTer7 | |
| XM_011514680.1:c.7713del | XP_011512982.1:p.His2572IlefsTer7 | |
| XM_011514681.1:c.7713del | XP_011512983.1:p.His2572IlefsTer7 | |
| XM_011514682.1:c.7713del | XP_011512984.1:p.His2572IlefsTer7 | |
| XM_011514683.1:c.7071del | XP_011512985.1:p.His2358IlefsTer7 | |
| XM_011514684.1:c.7002del | XP_011512986.1:p.His2335IlefsTer7 | |
| XM_011514685.1:c.7713del | XP_011512987.1:p.His2572IlefsTer7 | |
| XM_011514686.1:c.7713del | XP_011512988.1:p.His2572IlefsTer7 | |
| XM_011514687.1:c.7713del | XP_011512989.1:p.His2572IlefsTer7 | |
| XM_011514688.1:c.7713del | XP_011512990.1:p.His2572IlefsTer7 | |
| XM_011514689.1:c.7713del | XP_011512991.1:p.His2572IlefsTer7 | |
| XM_011514690.1:c.1788del | XP_011512992.1:p.His597IlefsTer7 | |
| XM_011514691.1:c.1788del | XP_011512993.1:p.His597IlefsTer7 | |
| XM_011514680.3:c.7713del | XP_011512982.1:p.His2572IlefsTer7 | |
| XM_011514682.3:c.7713del | XP_011512984.1:p.His2572IlefsTer7 | |
| XM_011514683.3:c.7071del | XP_011512985.1:p.His2358IlefsTer7 | |
| XM_011514684.3:c.7002del | XP_011512986.1:p.His2335IlefsTer7 | |
| XM_011514686.2:c.7713del | XP_011512988.1:p.His2572IlefsTer7 | |
| XM_011514688.2:c.7713del | XP_011512990.1:p.His2572IlefsTer7 | |
| XM_011514690.3:c.1788del | XP_011512992.1:p.His597IlefsTer7 | |
| XM_011514691.3:c.1788del | XP_011512993.1:p.His597IlefsTer7 | |
| XM_017010944.2:c.7713del | XP_016866433.1:p.His2572IlefsTer7 | |
| XM_017010945.2:c.7638del | XP_016866434.1:p.His2547IlefsTer7 | |
| XM_017010946.2:c.7713del | XP_016866435.1:p.His2572IlefsTer7 | |
| XM_017010947.2:c.7449del | XP_016866436.1:p.His2484IlefsTer7 | |
| XM_017010948.2:c.7002del | XP_016866437.1:p.His2335IlefsTer7 | |
| XM_017010949.2:c.5853del | XP_016866438.1:p.His1952IlefsTer7 | |
| XM_017010950.1:c.7713del | XP_016866439.1:p.His2572IlefsTer7 | |
| XM_017010951.1:c.7713del | XP_016866440.1:p.His2572IlefsTer7 | |
| XM_017010952.1:c.7713del | XP_016866441.1:p.His2572IlefsTer7 | |
| XR_001743469.1:n.7989del | ||
| NM_138694.4:c.7713del MANE Select | NP_619639.3:p.His2572IlefsTer7 | |
| NM_170724.3:c.7713del | NP_733842.2:p.His2572IlefsTer7 |