Linked Data
ClinVar Variation Id:
91525
dbSNP Id:
rs398122614
gnomAD v2:
13-32968976-T-C
gnomAD v3:
13-32394839-T-C
gnomAD v4:
13-32394839-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32394839T>C , CM000675.2:g.32394839T>C | GRCh38 |
| NC_000013.10:g.32968976T>C , CM000675.1:g.32968976T>C | GRCh37 |
| NC_000013.9:g.31866976T>C | NCBI36 |
| NG_012772.3:g.84360T>C , LRG_293:g.84360T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.9407T>C | ENSP00000434898.2:p.Leu3136Pro | |
| ENST00000528762.2:c.*774T>C | ENSP00000433168.2:n.*774T>C | |
| ENST00000530893.7:c.9038T>C | ENSP00000499438.2:p.Leu3013Pro | |
| ENST00000665585.2:c.*969T>C | ENSP00000499570.2:n.*969T>C | |
| ENST00000666593.2:c.*252T>C | ENSP00000499256.2:n.*252T>C | |
| ENST00000700202.2:c.9356T>C | ENSP00000514856.2:p.Leu3119Pro | |
| ENST00000700202.1:c.1823T>C | ENSP00000514856.1:p.Leu608Pro | |
| ENST00000700203.1:n.1534T>C | ||
| ENST00000380152.8:c.9407T>C MANE Select | ENSP00000369497.3:p.Leu3136Pro | |
| ENST00000544455.6:c.9407T>C | ENSP00000439902.1:p.Leu3136Pro | |
| ENST00000614259.2:c.9415T>C | ENSP00000506251.1:n.9415T>C | |
| ENST00000665585.1:c.2285T>C | ||
| ENST00000666593.1:c.429T>C | ENSP00000499256.1:n.429T>C | |
| ENST00000680887.1:c.9407T>C | ENSP00000505508.1:p.Leu3136Pro | |
| ENST00000380152.7:c.9407T>C | ENSP00000369497.3:p.Leu3136Pro | |
| ENST00000470094.1:c.364T>C | ||
| ENST00000544455.5:c.9407T>C | ENSP00000439902.1:p.Leu3136Pro | |
| NM_000059.3:c.9407T>C , LRG_293t1:c.9407T>C | NP_000050.2:p.Leu3136Pro | |
| XM_011535203.1:c.9407T>C | XP_011533505.1:p.Leu3136Pro | |
| XM_011535204.1:c.9311T>C | XP_011533506.1:p.Leu3104Pro | |
| NM_000059.4:c.9407T>C MANE Select | NP_000050.3:p.Leu3136Pro |