Linked Data
dbSNP Id:
rs938418383
gnomAD v2:
11-9225842-G-A
gnomAD v4:
11-9204295-G-A
COSMIC:
COSM1135268
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.9204295G>A , CM000673.2:g.9204295G>A | GRCh38 |
| NC_000011.9:g.9225842G>A , CM000673.1:g.9225842G>A | GRCh37 |
| NC_000011.8:g.9182418G>A | NCBI36 |
| NG_053019.1:g.66041C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328194.8:c.314C>T MANE Select | ENSP00000328524.3:p.Ala105Val | |
| ENST00000530780.2:c.*140C>T | ENSP00000433925.1:n.*140C>T | |
| ENST00000530867.2:n.103C>T | ||
| ENST00000532696.2:n.237C>T | ||
| ENST00000679446.1:n.235C>T | ||
| ENST00000679460.1:n.103C>T | ||
| ENST00000679568.1:c.314C>T | ENSP00000505860.1:p.Ala105Val | |
| ENST00000679745.1:n.103C>T | ||
| ENST00000679999.1:c.314C>T | ENSP00000505198.1:p.Ala105Val | |
| ENST00000680252.1:c.103C>T | ||
| ENST00000680294.1:c.314C>T | ENSP00000506113.1:p.Ala105Val | |
| ENST00000680470.1:c.314C>T | ENSP00000505975.1:p.Ala105Val | |
| ENST00000680554.1:c.26C>T | ENSP00000505621.1:p.Ala9Val | |
| ENST00000680576.1:n.103C>T | ||
| ENST00000680599.1:n.231C>T | ||
| ENST00000680742.1:c.314C>T | ENSP00000505206.1:p.Ala105Val | |
| ENST00000680885.1:n.235C>T | ||
| ENST00000681158.1:c.103C>T | ||
| ENST00000681173.1:n.103C>T | ||
| ENST00000681203.1:c.242C>T | ENSP00000506456.1:p.Ala81Val | |
| ENST00000681425.1:n.235C>T | ||
| ENST00000681915.1:n.103C>T | ||
| ENST00000328194.7:c.314C>T | ENSP00000328524.3:p.Ala105Val | |
| ENST00000526707.5:c.242C>T | ENSP00000436780.1:p.Ala81Val | |
| ENST00000530044.5:c.314C>T | ENSP00000435866.1:p.Ala105Val | |
| ENST00000530780.1:c.*140C>T | ENSP00000433925.1:n.*140C>T | |
| ENST00000532696.1:n.69C>T | ||
| NM_001243254.1:c.314C>T | NP_001230183.1:p.Ala105Val | |
| NM_015213.3:c.314C>T | NP_056028.2:p.Ala105Val | |
| XM_005252832.1:c.314C>T | XP_005252889.1:p.Ala105Val | |
| XM_011519952.1:c.314C>T | XP_011518254.1:p.Ala105Val | |
| XR_242782.2:n.579C>T | ||
| XR_930851.1:n.579C>T | ||
| XR_930852.1:n.579C>T | ||
| XR_930853.1:n.579C>T | ||
| NM_001348749.1:c.242C>T | NP_001335678.1:p.Ala81Val | |
| NM_001348750.1:c.26C>T | NP_001335679.1:p.Ala9Val | |
| NR_145966.2:n.571C>T | ||
| NM_015213.4:c.314C>T MANE Select | NP_056028.2:p.Ala105Val | |
| NM_001243254.2:c.314C>T | NP_001230183.1:p.Ala105Val | |
| NM_001348749.2:c.242C>T | NP_001335678.1:p.Ala81Val | |
| NM_001348750.2:c.26C>T | NP_001335679.1:p.Ala9Val |