Linked Data
ClinVar Variation Id:
166885
dbSNP Id:
rs147591591
ExAC:
4:47945275 G / A
gnomAD v2:
4-47945275-G-A
gnomAD v3:
4-47943258-G-A
gnomAD v4:
4-47943258-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47943258G>A , CM000666.2:g.47943258G>A | GRCh38 |
| NC_000004.11:g.47945275G>A , CM000666.1:g.47945275G>A | GRCh37 |
| NC_000004.10:g.47640032G>A | NCBI36 |
| NG_009193.1:g.74687C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000402813.9:c.360C>T (CNGA1) | ENSP00000384264.5:p.Asn120= | |
| ENST00000420489.7:c.360C>T (CNGA1) | ENSP00000389881.3:p.Asn120= | |
| ENST00000504722.6:c.360C>T (CNGA1) | ENSP00000423721.2:p.Asn120= | |
| ENST00000514170.7:c.360C>T (CNGA1) MANE Select | ENSP00000426862.3:p.Asn120= | |
| ENST00000358519.8:c.372C>T (CNGA1) | ENSP00000351320.4:p.Asn124= | |
| ENST00000402813.7:c.579C>T (CNGA1) | ENSP00000384264.3:p.Asn193= | |
| ENST00000420489.6:c.372C>T (CNGA1) | ENSP00000389881.2:p.Asn124= | |
| ENST00000500571.2:n.479-15766G>A (NIPAL1) | ||
| ENST00000504722.5:c.372C>T (CNGA1) | ENSP00000423721.1:p.Asn124= | |
| ENST00000506118.1:n.360C>T (CNGA1) | ||
| ENST00000513724.1:n.563+28554G>A (NIPAL1) | ||
| ENST00000514170.5:c.372C>T (CNGA1) | ENSP00000426862.1:p.Asn124= | |
| ENST00000544810.5:c.579C>T (CNGA1) | ENSP00000443401.2:p.Asn193= | |
| NM_000087.3:c.372C>T (CNGA1) | NP_000078.2:p.Asn124= | |
| NM_001142564.1:c.579C>T (CNGA1) | NP_001136036.1:p.Asn193= | |
| NR_125879.1:n.479-15766G>A | ||
| XM_005248049.3:c.372C>T (CNGA1) | XP_005248106.1:p.Asn124= | |
| XM_011513623.1:c.372C>T (CNGA1) | XP_011511925.1:p.Asn124= | |
| XM_005248049.4:c.597C>T (CNGA1) | XP_005248106.2:p.Asn199= | |
| XM_011513623.2:c.372C>T (CNGA1) | XP_011511925.1:p.Asn124= | |
| XM_017007712.1:c.372C>T (CNGA1) | XP_016863201.1:p.Asn124= | |
| NM_000087.4:c.372C>T (CNGA1) | NP_000078.2:p.Asn124= | |
| NM_001375386.1:c.372C>T (CNGA1) | NP_001362315.1:p.Asn124= | |
| NM_000087.5:c.360C>T (CNGA1) | NP_000078.3:p.Asn120= | |
| NM_001142564.2:c.360C>T (CNGA1) | NP_001136036.2:p.Asn120= | |
| NM_001379270.1:c.360C>T (CNGA1) MANE Select | NP_001366199.1:p.Asn120= |