HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31817155G>T , CM000668.2:g.31817155G>T | GRCh38 |
NC_000006.11:g.31784932G>T , CM000668.1:g.31784932G>T | GRCh37 |
NC_000006.10:g.31892911G>T | NCBI36 |
NG_011855.1:g.2904C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375651.7:c.1399G>T (HSPA1A) MANE Select | ENSP00000364802.5:p.Ala467Ser | |
ENST00000375651.6:c.1399G>T (HSPA1A) | ENSP00000364802.5:p.Ala467Ser | |
ENST00000608703.1:c.904G>T (HSPA1A) | ENSP00000477378.1:p.Ala302Ser | |
NM_005345.5:c.1399G>T (HSPA1A) | NP_005336.3:p.Ala467Ser | |
XM_005249073.2:c.-14+3858C>A (HSPA1L) | XP_005249130.1:n.-14+3858C>A | |
XM_011514566.1:c.-14+3858C>A (HSPA1L) | XP_011512868.1:n.-14+3858C>A | |
NM_005345.6:c.1399G>T (HSPA1A) MANE Select | NP_005336.3:p.Ala467Ser |