Linked Data
ClinVar Variation Id:
764816
ClinVar RCV Id:
RCV000943180
dbSNP Id:
rs1381046312
gnomAD v4:
22-46352311-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.46352311G>A , CM000684.2:g.46352311G>A | GRCh38 |
| NC_000022.10:g.46748208G>A , CM000684.1:g.46748208G>A | GRCh37 |
| NC_000022.9:g.45126872G>A | NCBI36 |
| NG_012173.1:g.21911G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465378.6:n.801G>A | ||
| ENST00000642923.1:c.648G>A | ENSP00000494255.1:p.Lys216= | |
| ENST00000643137.1:c.648G>A | ENSP00000495331.1:p.Lys216= | |
| ENST00000644006.1:c.*197G>A | ENSP00000493778.1:n.*197G>A | |
| ENST00000645026.1:n.804G>A | ||
| ENST00000645190.1:c.753G>A MANE Select | ENSP00000496496.1:p.Lys251= | |
| ENST00000647301.1:c.*197G>A | ENSP00000496641.1:n.*197G>A | |
| ENST00000290846.8:c.753G>A | ENSP00000290846.4:p.Lys251= | |
| ENST00000381019.3:c.753G>A | ENSP00000370407.3:p.Lys251= | |
| ENST00000381021.7:c.*346G>A | ENSP00000370409.3:n.*346G>A | |
| ENST00000441818.5:c.*287G>A | ENSP00000393014.1:n.*287G>A | |
| ENST00000453630.5:c.*291G>A | ENSP00000398488.1:n.*291G>A | |
| ENST00000456595.5:c.*287G>A | ENSP00000413880.1:n.*287G>A | |
| ENST00000457572.5:c.*197G>A | ENSP00000407700.1:n.*197G>A | |
| ENST00000463785.1:n.221G>A | ||
| ENST00000479648.1:n.573G>A | ||
| ENST00000485175.5:n.713G>A | ||
| ENST00000486620.5:n.795G>A | ||
| NM_001282782.1:c.411G>A | NP_001269711.1:p.Lys137= | |
| NM_001282783.1:c.333G>A | NP_001269712.1:p.Lys111= | |
| NM_001282784.1:c.333G>A | NP_001269713.1:p.Lys111= | |
| NM_001282785.1:c.753G>A | NP_001269714.1:p.Lys251= | |
| NM_018006.4:c.753G>A | NP_060476.2:p.Lys251= | |
| NR_104240.1:n.1062G>A | ||
| NR_104241.1:n.955G>A | ||
| XM_005261678.1:c.357G>A | XP_005261735.1:p.Lys119= | |
| XM_005261681.1:c.357G>A | XP_005261738.1:p.Lys119= | |
| XM_011530271.1:c.648G>A | XP_011528573.1:p.Lys216= | |
| XM_011530272.1:c.753G>A | XP_011528574.1:p.Lys251= | |
| XM_011530273.1:c.753G>A | XP_011528575.1:p.Lys251= | |
| XM_011530274.1:c.411G>A | XP_011528576.1:p.Lys137= | |
| XM_011530275.1:c.357G>A | XP_011528577.1:p.Lys119= | |
| XM_011530271.2:c.648G>A | XP_011528573.1:p.Lys216= | |
| XM_011530272.2:c.753G>A | XP_011528574.1:p.Lys251= | |
| XM_011530273.2:c.753G>A | XP_011528575.1:p.Lys251= | |
| XM_011530274.2:c.411G>A | XP_011528576.1:p.Lys137= | |
| XM_024452260.1:c.648G>A | XP_024308028.1:p.Lys216= | |
| XR_001755261.2:n.799G>A | ||
| XR_001755262.2:n.799G>A | ||
| NM_018006.5:c.753G>A MANE Select | NP_060476.2:p.Lys251= | |
| NM_001282782.2:c.411G>A | NP_001269711.1:p.Lys137= | |
| NM_001282783.2:c.333G>A | NP_001269712.1:p.Lys111= | |
| NM_001282784.2:c.333G>A | NP_001269713.1:p.Lys111= | |
| NM_001282785.2:c.753G>A | NP_001269714.1:p.Lys251= | |
| NR_104240.2:n.749G>A | ||
| NR_104241.2:n.642G>A |