Revel Score:
ENST00000374708
0.714
ENST00000341947 (MANE Select)
0.714
ENST00000357486
0.714
ENST00000374714
0.714
ENST00000374713
0.714
ENST00000395197
0.714
ENST00000374712
0.714
ENST00000361917
0.714
gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00001774 (EAS)
Exomes Max Group AF
0.00002003 (EAS)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33172580G>A , CM000668.2:g.33172580G>A | GRCh38 |
| NC_000006.11:g.33140357G>A , CM000668.1:g.33140357G>A | GRCh37 |
| NC_000006.10:g.33248335G>A | NCBI36 |
| NG_011589.1:g.24889C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341947.7:c.2848C>T MANE Select | ENSP00000339915.2:p.Pro950Ser | |
| ENST00000341947.6:c.2848C>T | ENSP00000339915.2:p.Pro950Ser | |
| ENST00000361917.5:c.2527C>T | ENSP00000355123.1:p.Pro843Ser | |
| ENST00000374708.8:c.2590C>T | ENSP00000363840.4:p.Pro864Ser | |
| ENST00000477772.1:n.272+4429C>T | ||
| NM_080679.2:c.2527C>T | NP_542410.2:p.Pro843Ser | |
| NM_080680.2:c.2848C>T | NP_542411.2:p.Pro950Ser | |
| NM_080681.2:c.2590C>T | NP_542412.2:p.Pro864Ser | |
| XM_011514298.1:c.2002C>T | XP_011512600.1:p.Pro668Ser | |
| XM_011514299.1:c.2134C>T | XP_011512601.1:p.Pro712Ser | |
| XM_011514300.1:c.1954C>T | XP_011512602.1:p.Pro652Ser | |
| XM_011514301.1:c.1891C>T | XP_011512603.1:p.Pro631Ser | |
| XM_011514302.1:c.1735C>T | XP_011512604.1:p.Pro579Ser | |
| XM_011514299.2:c.2134C>T | XP_011512601.1:p.Pro712Ser | |
| XM_011514300.2:c.1954C>T | XP_011512602.1:p.Pro652Ser | |
| XM_011514302.2:c.1735C>T | XP_011512604.1:p.Pro579Ser | |
| XM_017010250.1:c.2848C>T | XP_016865739.1:p.Pro950Ser | |
| XM_017010251.2:c.1666C>T | XP_016865740.1:p.Pro556Ser | |
| NM_080680.3:c.2848C>T MANE Select | NP_542411.2:p.Pro950Ser | |
| NM_080681.3:c.2590C>T | NP_542412.2:p.Pro864Ser | |
| NM_080679.3:c.2527C>T | NP_542410.2:p.Pro843Ser |