Linked Data
ClinVar Variation Id:
2156835
ClinVar RCV Id:
RCV003079433
dbSNP Id:
rs200453149
ExAC:
7:92123708 C / T
gnomAD v2:
7-92123708-C-T
gnomAD v3:
7-92494394-C-T
gnomAD v4:
7-92494394-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92494394C>T , CM000669.2:g.92494394C>T | GRCh38 |
| NC_000007.13:g.92123708C>T , CM000669.1:g.92123708C>T | GRCh37 |
| NC_000007.12:g.91961644C>T | NCBI36 |
| NG_008341.1:g.39138G>A | |
| NG_008341.2:g.39138G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.2929G>A (PEX1) MANE Select | ENSP00000248633.4:p.Val977Ile | |
| ENST00000248633.8:c.2929G>A (PEX1) | ENSP00000248633.4:p.Val977Ile | |
| ENST00000428214.5:c.2758G>A (PEX1) | ENSP00000394413.1:p.Val920Ile | |
| ENST00000438045.5:c.1963G>A (PEX1) | ENSP00000410438.1:p.Val655Ile | |
| ENST00000484913.5:n.2968G>A (PEX1) | ||
| ENST00000496420.5:n.2821G>A (PEX1) | ||
| NM_000466.2:c.2929G>A (PEX1) | NP_000457.1:p.Val977Ile | |
| NM_001282677.1:c.2758G>A (PEX1) | NP_001269606.1:p.Val920Ile | |
| NM_001282678.1:c.2305G>A (PEX1) | NP_001269607.1:p.Val769Ile | |
| XM_005250433.3:c.1180G>A (PEX1) | XP_005250490.1:p.Val394Ile | |
| XR_242246.3:n.3025G>A (PEX1) | ||
| XM_017012319.2:c.1180G>A (PEX1) | XP_016867808.1:p.Val394Ile | |
| XR_001744808.2:n.1956G>A (PEX1) | ||
| XR_001744843.2:n.5363C>T (GATAD1) | ||
| XR_242246.5:n.2976G>A (PEX1) | ||
| XR_927494.3:n.4214C>T (GATAD1) | ||
| XR_927503.3:n.4145C>T (GATAD1) | ||
| NM_000466.3:c.2929G>A (PEX1) MANE Select | NP_000457.1:p.Val977Ile | |
| NM_001282677.2:c.2758G>A (PEX1) | NP_001269606.1:p.Val920Ile | |
| NM_001282678.2:c.2305G>A (PEX1) | NP_001269607.1:p.Val769Ile |