Linked Data
ClinVar Variation Id:
2413348
ClinVar RCV Id:
RCV003110351
dbSNP Id:
rs1791533094
MyVariant Identifiers:
chr7:g.92123688A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92494374A>G , CM000669.2:g.92494374A>G | GRCh38 |
| NC_000007.13:g.92123688A>G , CM000669.1:g.92123688A>G | GRCh37 |
| NC_000007.12:g.91961624A>G | NCBI36 |
| NG_008341.1:g.39158T>C | |
| NG_008341.2:g.39158T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.2949T>C (PEX1) MANE Select | ENSP00000248633.4:p.Thr983= | |
| ENST00000248633.8:c.2949T>C (PEX1) | ENSP00000248633.4:p.Thr983= | |
| ENST00000428214.5:c.2778T>C (PEX1) | ENSP00000394413.1:p.Thr926= | |
| ENST00000438045.5:c.1983T>C (PEX1) | ENSP00000410438.1:p.Thr661= | |
| ENST00000484913.5:n.2988T>C (PEX1) | ||
| ENST00000496420.5:n.2841T>C (PEX1) | ||
| NM_000466.2:c.2949T>C (PEX1) | NP_000457.1:p.Thr983= | |
| NM_001282677.1:c.2778T>C (PEX1) | NP_001269606.1:p.Thr926= | |
| NM_001282678.1:c.2325T>C (PEX1) | NP_001269607.1:p.Thr775= | |
| XM_005250433.3:c.1200T>C (PEX1) | XP_005250490.1:p.Thr400= | |
| XR_242246.3:n.3045T>C (PEX1) | ||
| XM_017012319.2:c.1200T>C (PEX1) | XP_016867808.1:p.Thr400= | |
| XR_001744808.2:n.1976T>C (PEX1) | ||
| XR_001744843.2:n.5343A>G (GATAD1) | ||
| XR_242246.5:n.2996T>C (PEX1) | ||
| XR_927494.3:n.4194A>G (GATAD1) | ||
| XR_927503.3:n.4125A>G (GATAD1) | ||
| NM_000466.3:c.2949T>C (PEX1) MANE Select | NP_000457.1:p.Thr983= | |
| NM_001282677.2:c.2778T>C (PEX1) | NP_001269606.1:p.Thr926= | |
| NM_001282678.2:c.2325T>C (PEX1) | NP_001269607.1:p.Thr775= |