Revel Score:
ENST00000375651 (MANE Select)
0.105
ENST00000541556
0.105
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31816086G>T , CM000668.2:g.31816086G>T | GRCh38 |
| NC_000006.11:g.31783863G>T , CM000668.1:g.31783863G>T | GRCh37 |
| NC_000006.10:g.31891842G>T | NCBI36 |
| NG_011855.1:g.3973C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375651.7:c.330G>T (HSPA1A) MANE Select | ENSP00000364802.5:p.Glu110Asp | |
| ENST00000375651.6:c.330G>T (HSPA1A) | ENSP00000364802.5:p.Glu110Asp | |
| ENST00000608703.1:c.76-241G>T (HSPA1A) | ENSP00000477378.1:n.76-241G>T | |
| NM_005345.5:c.330G>T (HSPA1A) | NP_005336.3:p.Glu110Asp | |
| XM_005249073.2:c.-13-4101C>A (HSPA1L) | XP_005249130.1:n.-13-4101C>A | |
| XM_011514566.1:c.-13-4101C>A (HSPA1L) | XP_011512868.1:n.-13-4101C>A | |
| NM_005345.6:c.330G>T (HSPA1A) MANE Select | NP_005336.3:p.Glu110Asp |