Linked Data
ClinVar Variation Id:
2730570
ClinVar RCV Id:
RCV003508729
gnomAD v4:
5-132390849-C-T
MyVariant Identifiers:
chr5:g.131726541C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132390849C>T , CM000667.2:g.132390849C>T | GRCh38 |
| NC_000005.9:g.131726541C>T , CM000667.1:g.131726541C>T | GRCh37 |
| NC_000005.8:g.131754440C>T | NCBI36 |
| NG_008982.1:g.26141C>T | |
| NG_008982.2:g.26146C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415928.6:c.1053C>T | ENSP00000388838.2:p.Ala351= | |
| ENST00000435065.7:c.1284C>T | ENSP00000402760.2:p.Ala428= | |
| ENST00000448810.6:c.*64C>T | ENSP00000401860.2:n.*64C>T | |
| ENST00000685543.1:n.1353C>T | ||
| ENST00000686757.1:c.*376C>T | ENSP00000510721.1:n.*376C>T | |
| ENST00000687740.1:n.3897C>T | ||
| ENST00000688151.1:n.2522C>T | ||
| ENST00000689271.1:c.1059C>T | ENSP00000510797.1:p.Ala353= | |
| ENST00000690900.1:c.*376C>T | ENSP00000510703.1:n.*376C>T | |
| ENST00000692212.1:n.2824C>T | ||
| ENST00000692355.1:c.465C>T | ||
| ENST00000692413.1:c.1194C>T | ENSP00000509374.1:p.Ala398= | |
| ENST00000692825.1:c.1280C>T | ENSP00000509447.1:n.1280C>T | |
| ENST00000693308.1:c.1260C>T | ENSP00000509770.1:p.Ala420= | |
| ENST00000693763.1:n.2372C>T | ||
| ENST00000245407.8:c.1212C>T MANE Select | ENSP00000245407.3:p.Ala404= | |
| ENST00000245407.7:c.1212C>T | ENSP00000245407.3:p.Ala404= | |
| ENST00000435065.6:c.1284C>T | ENSP00000402760.2:p.Ala428= | |
| ENST00000447841.5:c.112-1584C>T | ||
| ENST00000448810.5:c.474C>T | ||
| ENST00000461013.5:n.8634C>T | ||
| ENST00000475308.1:n.1890C>T | ||
| ENST00000479605.5:n.315C>T | ||
| NM_001308122.1:c.1284C>T | NP_001295051.1:p.Ala428= | |
| NM_003060.3:c.1212C>T | NP_003051.1:p.Ala404= | |
| XM_011543590.1:c.594C>T | XP_011541892.1:p.Ala198= | |
| XR_427718.1:n.1572C>T | ||
| XR_948290.1:n.1394-1584C>T | ||
| XR_948291.1:n.1566C>T | ||
| XM_011543590.2:c.594C>T | XP_011541892.1:p.Ala198= | |
| XM_017009778.2:c.684C>T | XP_016865267.1:p.Ala228= | |
| XR_001742215.1:n.1467C>T | ||
| XR_001742216.1:n.1486C>T | ||
| XR_427718.2:n.1572C>T | ||
| XR_948290.2:n.1394-1584C>T | ||
| XR_948291.2:n.1566C>T | ||
| NM_003060.4:c.1212C>T MANE Select | NP_003051.1:p.Ala404= | |
| NM_001308122.2:c.1284C>T | NP_001295051.1:p.Ala428= |