Linked Data
dbSNP Id:
rs1752783825
gnomAD v3:
5-132393734-C-T
gnomAD v4:
5-132393734-C-T
MyVariant Identifiers:
chr5:g.131729426C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132393734C>T , CM000667.2:g.132393734C>T | GRCh38 |
| NC_000005.9:g.131729426C>T , CM000667.1:g.131729426C>T | GRCh37 |
| NC_000005.8:g.131757325C>T | NCBI36 |
| NG_008982.1:g.29026C>T | |
| NG_008982.2:g.29031C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415928.6:c.1292-451C>T | ENSP00000388838.2:n.1292-451C>T | |
| ENST00000435065.7:c.1581C>T | ENSP00000402760.2:p.Ala527= | |
| ENST00000448810.6:c.*361C>T | ENSP00000401860.2:n.*361C>T | |
| ENST00000685543.1:n.1650C>T | ||
| ENST00000686757.1:c.*673C>T | ENSP00000510721.1:n.*673C>T | |
| ENST00000686868.1:n.501C>T | ||
| ENST00000687740.1:n.4194C>T | ||
| ENST00000688151.1:n.2819C>T | ||
| ENST00000689271.1:c.1356C>T | ENSP00000510797.1:p.Ala452= | |
| ENST00000690900.1:c.*673C>T | ENSP00000510703.1:n.*673C>T | |
| ENST00000692212.1:n.4649C>T | ||
| ENST00000692355.1:c.762C>T | ||
| ENST00000692413.1:c.1491C>T | ENSP00000509374.1:p.Ala497= | |
| ENST00000692825.1:c.1577C>T | ENSP00000509447.1:n.1577C>T | |
| ENST00000693308.1:c.1557C>T | ENSP00000509770.1:p.Ala519= | |
| ENST00000693763.1:n.2669C>T | ||
| ENST00000245407.8:c.1509C>T MANE Select | ENSP00000245407.3:p.Ala503= | |
| ENST00000245407.7:c.1509C>T | ENSP00000245407.3:p.Ala503= | |
| ENST00000435065.6:c.1581C>T | ENSP00000402760.2:p.Ala527= | |
| ENST00000447841.5:c.353C>T | ||
| ENST00000448810.5:c.771C>T | ||
| ENST00000461013.5:n.8931C>T | ||
| ENST00000475308.1:n.2187C>T | ||
| NM_001308122.1:c.1581C>T | NP_001295051.1:p.Ala527= | |
| NM_003060.3:c.1509C>T | NP_003051.1:p.Ala503= | |
| XM_011543590.1:c.891C>T | XP_011541892.1:p.Ala297= | |
| XR_948290.1:n.1635C>T | ||
| XM_011543590.2:c.891C>T | XP_011541892.1:p.Ala297= | |
| XM_017009778.2:c.981C>T | XP_016865267.1:p.Ala327= | |
| XR_001742215.1:n.1764C>T | ||
| XR_001742216.1:n.1783C>T | ||
| XR_427718.2:n.1869C>T | ||
| XR_948290.2:n.1635C>T | ||
| XR_948291.2:n.1863C>T | ||
| NM_003060.4:c.1509C>T MANE Select | NP_003051.1:p.Ala503= | |
| NM_001308122.2:c.1581C>T | NP_001295051.1:p.Ala527= |