Revel Score:
ENST00000295897 (MANE Select)
0.499
ENST00000415165
0.499
ENST00000503124
0.499
ENST00000509063
0.499
ENST00000401494
0.499
ENST00000430202
0.499
ENST00000511370
0.134
gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73412027A>G , CM000666.2:g.73412027A>G | GRCh38 |
| NC_000004.11:g.74277744A>G , CM000666.1:g.74277744A>G | GRCh37 |
| NC_000004.10:g.74496608A>G | NCBI36 |
| NG_009291.1:g.12773A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295897.9:c.745A>G MANE Select | ENSP00000295897.4:p.Lys249Glu | |
| ENST00000295897.8:c.745A>G | ENSP00000295897.4:p.Lys249Glu | |
| ENST00000401494.7:c.400A>G | ENSP00000384695.3:p.Lys134Glu | |
| ENST00000415165.6:c.169A>G | ENSP00000401820.2:p.Lys57Glu | |
| ENST00000476441.6:c.*24A>G | ENSP00000423727.1:n.*24A>G | |
| ENST00000503124.5:c.295A>G | ENSP00000421027.1:p.Lys99Glu | |
| ENST00000505649.5:n.431A>G | ||
| ENST00000507673.1:n.62A>G | ||
| ENST00000509063.5:c.745A>G | ENSP00000422784.1:p.Lys249Glu | |
| ENST00000511370.1:c.278A>G | ||
| ENST00000621085.4:c.490+2665A>G | ENSP00000483421.1:n.490+2665A>G | |
| ENST00000621628.4:c.486+2951A>G | ENSP00000480485.1:n.486+2951A>G | |
| NM_000477.5:c.745A>G | NP_000468.1:p.Lys249Glu | |
| NM_000477.6:c.745A>G | NP_000468.1:p.Lys249Glu | |
| NM_000477.7:c.745A>G MANE Select | NP_000468.1:p.Lys249Glu |