Linked Data
dbSNP Id:
rs200156944
gnomAD v3:
13-32376521-C-CAAAAAAA
gnomAD v4:
13-32376521-C-CAAAAAAA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32376529_32376535dup , CM000675.2:g.32376529_32376535dup | GRCh38 |
| NC_000013.10:g.32950666_32950672dup , CM000675.1:g.32950666_32950672dup | GRCh37 |
| NC_000013.9:g.31848666_31848672dup | NCBI36 |
| NG_012772.3:g.66050_66056dup , LRG_293:g.66050_66056dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.8633-141_8633-135dup | ENSP00000434898.2:n.8633-141_8633-135dup | |
| ENST00000528762.2:c.8697-141_8697-135dup | ENSP00000433168.2:n.8697-141_8697-135dup | |
| ENST00000530893.7:c.8264-141_8264-135dup | ENSP00000499438.2:n.8264-141_8264-135dup | |
| ENST00000665585.2:c.*195-141_*195-135dup | ENSP00000499570.2:n.*195-141_*195-135dup | |
| ENST00000666593.2:c.8633-141_8633-135dup | ENSP00000499256.2:n.8633-141_8633-135dup | |
| ENST00000700202.2:c.8633-141_8633-135dup | ENSP00000514856.2:n.8633-141_8633-135dup | |
| ENST00000700202.1:c.1100-141_1100-135dup | ENSP00000514856.1:n.1100-141_1100-135dup | |
| ENST00000700203.1:n.619_625dup | ||
| ENST00000380152.8:c.8633-141_8633-135dup MANE Select | ENSP00000369497.3:n.8633-141_8633-135dup | |
| ENST00000544455.6:c.8633-141_8633-135dup | ENSP00000439902.1:n.8633-141_8633-135dup | |
| ENST00000614259.2:c.8641-141_8641-135dup | ENSP00000506251.1:n.8641-141_8641-135dup | |
| ENST00000665585.1:c.1511-141_1511-135dup | ||
| ENST00000680887.1:c.8633-141_8633-135dup | ENSP00000505508.1:n.8633-141_8633-135dup | |
| ENST00000380152.7:c.8633-141_8633-135dup | ENSP00000369497.3:n.8633-141_8633-135dup | |
| ENST00000528762.1:c.195-141_195-135dup | ENSP00000433168.1:n.195-141_195-135dup | |
| ENST00000544455.5:c.8633-141_8633-135dup | ENSP00000439902.1:n.8633-141_8633-135dup | |
| NM_000059.3:c.8633-141_8633-135dup , LRG_293t1:c.8633-141_8633-135dup | NP_000050.2:n.8633-141_8633-135dup | |
| XM_011535203.1:c.8633-141_8633-135dup | XP_011533505.1:n.8633-141_8633-135dup | |
| XM_011535204.1:c.8537-141_8537-135dup | XP_011533506.1:n.8537-141_8537-135dup | |
| XM_011535205.1:c.8633-141_8633-135dup | XP_011533507.1:n.8633-141_8633-135dup | |
| NM_000059.4:c.8633-141_8633-135dup MANE Select | NP_000050.3:n.8633-141_8633-135dup |