HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31816561A>T , CM000668.2:g.31816561A>T | GRCh38 |
NC_000006.11:g.31784338A>T , CM000668.1:g.31784338A>T | GRCh37 |
NC_000006.10:g.31892317A>T | NCBI36 |
NG_011855.1:g.3498T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375651.7:c.805A>T (HSPA1A) MANE Select | ENSP00000364802.5:p.Arg269Trp | |
ENST00000375651.6:c.805A>T (HSPA1A) | ENSP00000364802.5:p.Arg269Trp | |
ENST00000608703.1:c.310A>T (HSPA1A) | ENSP00000477378.1:p.Arg104Trp | |
NM_005345.5:c.805A>T (HSPA1A) | NP_005336.3:p.Arg269Trp | |
XM_005249073.2:c.-14+4452T>A (HSPA1L) | XP_005249130.1:n.-14+4452T>A | |
XM_011514566.1:c.-14+4452T>A (HSPA1L) | XP_011512868.1:n.-14+4452T>A | |
NM_005345.6:c.805A>T (HSPA1A) MANE Select | NP_005336.3:p.Arg269Trp |