Linked Data
dbSNP Id:
rs1203519733
gnomAD v2:
5-131633361-C-CA
gnomAD v3:
5-132297668-C-CA
gnomAD v4:
5-132297668-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132297673dup , CM000667.2:g.132297673dup | GRCh38 |
| NC_000005.9:g.131633366dup , CM000667.1:g.131633366dup | GRCh37 |
| NC_000005.8:g.131661265dup | NCBI36 |
| NG_012129.1:g.8222dup | |
| NG_012129.2:g.8222dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000200652.4:c.393+2664dup MANE Select | ENSP00000200652.3:n.393+2664dup | |
| ENST00000200652.3:c.393+2664dup | ENSP00000200652.3:n.393+2664dup | |
| ENST00000491257.1:n.197+2052dup | ||
| NM_003059.2:c.393+2664dup | NP_003050.2:n.393+2664dup | |
| XM_006714675.2:c.-32+2664dup | XP_006714738.1:n.-32+2664dup | |
| XM_011543589.1:c.393+2664dup | XP_011541891.1:n.393+2664dup | |
| XR_948289.1:n.1238+2052dup | ||
| XM_006714675.4:c.-32+2664dup | XP_006714738.1:n.-32+2664dup | |
| XM_011543589.2:c.393+2664dup | XP_011541891.1:n.393+2664dup | |
| XM_017009776.1:c.-136+2052dup | XP_016865265.1:n.-136+2052dup | |
| NM_003059.3:c.393+2664dup MANE Select | NP_003050.2:n.393+2664dup |