Linked Data
dbSNP Id:
rs368429047
ExAC:
X:153641610 C / T
gnomAD v2:
X-153641610-C-T
gnomAD v3:
X-154413273-C-T
gnomAD v4:
X-154413273-C-T
COSMIC:
COSN1085088
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154413273C>T , CM000685.2:g.154413273C>T | GRCh38 |
| NC_000023.10:g.153641610C>T , CM000685.1:g.153641610C>T | GRCh37 |
| NC_000023.9:g.153294804C>T | NCBI36 |
| NG_009634.1:g.6734C>T | |
| NG_012884.2:g.3816G>A | |
| NG_009634.2:g.6739C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698234.1:n.733C>T | ||
| ENST00000698235.1:n.292C>T | ||
| ENST00000698317.1:n.1259C>T | ||
| ENST00000698318.1:n.1120C>T | ||
| ENST00000470127.2:n.354C>T | ||
| ENST00000475699.6:c.338+21C>T | ENSP00000419854.3:n.338+21C>T | |
| ENST00000476800.2:n.1262C>T | ||
| ENST00000483674.3:n.175+21C>T | ||
| ENST00000601016.6:c.284+21C>T MANE Select | ENSP00000469981.1:n.284+21C>T | |
| ENST00000612012.5:c.284+21C>T | ENSP00000482070.2:n.284+21C>T | |
| ENST00000612460.5:c.284+21C>T | ENSP00000481037.1:n.284+21C>T | |
| ENST00000614595.2:n.1655C>T | ||
| ENST00000615658.5:n.597+21C>T | ||
| ENST00000616020.5:c.338+21C>T | ENSP00000483636.2:n.338+21C>T | |
| ENST00000617701.5:c.*17C>T | ENSP00000481645.1:n.*17C>T | |
| ENST00000621647.2:n.358C>T | ||
| ENST00000652354.1:c.8+21C>T | ENSP00000498734.1:n.8+21C>T | |
| ENST00000652358.1:c.11C>T | ENSP00000498464.1:p.Ser4Leu | |
| ENST00000652390.1:c.203+21C>T | ENSP00000498858.1:n.203+21C>T | |
| ENST00000652476.1:n.466C>T | ||
| ENST00000652682.1:c.284+21C>T | ENSP00000498288.1:n.284+21C>T | |
| ENST00000652685.1:n.357C>T | ||
| ENST00000369776.8:c.209+21C>T | ENSP00000358791.4:n.209+21C>T | |
| ENST00000426231.5:c.121C>T | ||
| ENST00000439735.2:c.284+21C>T | ENSP00000398193.1:n.284+21C>T | |
| ENST00000475699.5:c.284+21C>T | ENSP00000419854.2:n.284+21C>T | |
| ENST00000476679.5:n.197+21C>T | ||
| ENST00000476800.1:n.183C>T | ||
| ENST00000479875.1:n.313+21C>T | ||
| ENST00000483780.5:n.58+21C>T | ||
| ENST00000601016.5:c.284+21C>T | ENSP00000469981.1:n.284+21C>T | |
| ENST00000612012.4:c.338+21C>T | ENSP00000482070.1:n.338+21C>T | |
| ENST00000612460.4:c.284+21C>T | ENSP00000481037.1:n.284+21C>T | |
| ENST00000613002.4:c.284+21C>T | ENSP00000478154.1:n.284+21C>T | |
| ENST00000613634.4:n.604+21C>T | ||
| ENST00000615658.4:n.631C>T | ||
| ENST00000615986.4:c.*17C>T | ENSP00000480133.1:n.*17C>T | |
| ENST00000616020.4:c.338+21C>T | ENSP00000483636.1:n.338+21C>T | |
| ENST00000617701.4:c.*17C>T | ENSP00000481645.1:n.*17C>T | |
| ENST00000620808.4:c.*17C>T | ENSP00000479311.1:n.*17C>T | |
| ENST00000621647.1:n.590C>T | ||
| NM_000116.4:c.284+21C>T | NP_000107.1:n.284+21C>T | |
| NM_001303465.1:c.338+21C>T | NP_001290394.1:n.338+21C>T | |
| NM_181311.3:c.284+21C>T | NP_851828.1:n.284+21C>T | |
| NM_181312.3:c.284+21C>T | NP_851829.1:n.284+21C>T | |
| NM_181313.3:c.284+21C>T | NP_851830.1:n.284+21C>T | |
| NR_024048.2:n.631C>T | ||
| XM_006724836.1:c.338+21C>T | XP_006724899.1:n.338+21C>T | |
| XM_006724837.1:c.338+21C>T | XP_006724900.1:n.338+21C>T | |
| XM_006724839.1:c.338+21C>T | XP_006724902.1:n.338+21C>T | |
| XM_006724841.2:c.11C>T | XP_006724904.1:p.Ser4Leu | |
| XM_006724842.2:c.11C>T | XP_006724905.1:p.Ser4Leu | |
| XM_011531189.1:c.338+21C>T | XP_011529491.1:n.338+21C>T | |
| XM_011531190.1:c.11C>T | XP_011529492.1:p.Ser4Leu | |
| XM_011531191.1:c.8+21C>T | XP_011529493.1:n.8+21C>T | |
| XM_011531192.1:c.-93C>T | XP_011529494.1:n.-93C>T | |
| XR_938511.1:n.641+21C>T | ||
| XM_006724841.4:c.11C>T | XP_006724904.1:p.Ser4Leu | |
| XM_006724842.4:c.11C>T | XP_006724905.1:p.Ser4Leu | |
| XM_011531191.2:c.8+21C>T | XP_011529493.1:n.8+21C>T | |
| XM_017029761.1:c.284+21C>T | XP_016885250.1:n.284+21C>T | |
| XM_017029762.1:c.338+21C>T | XP_016885251.1:n.338+21C>T | |
| XM_017029763.1:c.284+21C>T | XP_016885252.1:n.284+21C>T | |
| XM_017029764.1:c.-93C>T | XP_016885253.1:n.-93C>T | |
| XM_017029765.2:c.11C>T | XP_016885254.1:p.Ser4Leu | |
| XM_024452431.1:c.338+21C>T | XP_024308199.1:n.338+21C>T | |
| NM_000116.5:c.284+21C>T MANE Select | NP_000107.1:n.284+21C>T | |
| NM_001303465.2:c.338+21C>T | NP_001290394.1:n.338+21C>T | |
| NM_181311.4:c.284+21C>T | NP_851828.1:n.284+21C>T | |
| NM_181312.4:c.284+21C>T | NP_851829.1:n.284+21C>T | |
| NM_181313.4:c.284+21C>T | NP_851830.1:n.284+21C>T | |
| NR_024048.3:n.610C>T |