Linked Data
ClinVar Variation Id:
1132010
ClinVar RCV Id:
RCV001466068
dbSNP Id:
rs1482170065
gnomAD v4:
4-47936658-G-A
MyVariant Identifiers:
chr4:g.47938675G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47936658G>A , CM000666.2:g.47936658G>A | GRCh38 |
| NC_000004.11:g.47938675G>A , CM000666.1:g.47938675G>A | GRCh37 |
| NC_000004.10:g.47633432G>A | NCBI36 |
| NG_009193.1:g.81287C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000402813.9:c.1824C>T (CNGA1) | ENSP00000384264.5:p.Asn608= | |
| ENST00000420489.7:c.1824C>T (CNGA1) | ENSP00000389881.3:p.Asn608= | |
| ENST00000514170.7:c.1824C>T (CNGA1) MANE Select | ENSP00000426862.3:p.Asn608= | |
| ENST00000358519.8:c.1836C>T (CNGA1) | ENSP00000351320.4:p.Asn612= | |
| ENST00000402813.7:c.2043C>T (CNGA1) | ENSP00000384264.3:p.Asn681= | |
| ENST00000420489.6:c.1836C>T (CNGA1) | ENSP00000389881.2:p.Asn612= | |
| ENST00000500571.2:n.478+21954G>A (NIPAL1) | ||
| ENST00000513724.1:n.563+21954G>A (NIPAL1) | ||
| ENST00000514170.5:c.1836C>T (CNGA1) | ENSP00000426862.1:p.Asn612= | |
| ENST00000544810.5:c.2043C>T (CNGA1) | ENSP00000443401.2:p.Asn681= | |
| NM_000087.3:c.1836C>T (CNGA1) | NP_000078.2:p.Asn612= | |
| NM_001142564.1:c.2043C>T (CNGA1) | NP_001136036.1:p.Asn681= | |
| NR_125879.1:n.478+21954G>A | ||
| XM_005248049.3:c.1836C>T (CNGA1) | XP_005248106.1:p.Asn612= | |
| XM_011513623.1:c.1836C>T (CNGA1) | XP_011511925.1:p.Asn612= | |
| XM_005248049.4:c.2061C>T (CNGA1) | XP_005248106.2:p.Asn687= | |
| XM_011513623.2:c.1836C>T (CNGA1) | XP_011511925.1:p.Asn612= | |
| XM_017007712.1:c.1836C>T (CNGA1) | XP_016863201.1:p.Asn612= | |
| NM_000087.4:c.1836C>T (CNGA1) | NP_000078.2:p.Asn612= | |
| NM_001375386.1:c.1836C>T (CNGA1) | NP_001362315.1:p.Asn612= | |
| NM_000087.5:c.1824C>T (CNGA1) | NP_000078.3:p.Asn608= | |
| NM_001142564.2:c.1824C>T (CNGA1) | NP_001136036.2:p.Asn608= | |
| NM_001379270.1:c.1824C>T (CNGA1) MANE Select | NP_001366199.1:p.Asn608= |