Canonical Allele Identifier: CA363415038
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816862T>C , CM000668.2:g.31816862T>C GRCh38
NC_000006.11:g.31784639T>C , CM000668.1:g.31784639T>C GRCh37
NC_000006.10:g.31892618T>C NCBI36
NG_011855.1:g.3197A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1106T>C (HSPA1A) MANE Select ENSP00000364802.5:p.Val369Ala
ENST00000375651.6:c.1106T>C (HSPA1A) ENSP00000364802.5:p.Val369Ala
ENST00000608703.1:c.611T>C (HSPA1A) ENSP00000477378.1:p.Val204Ala
NM_005345.5:c.1106T>C (HSPA1A) NP_005336.3:p.Val369Ala
XM_005249073.2:c.-14+4151A>G (HSPA1L) XP_005249130.1:n.-14+4151A>G
XM_011514566.1:c.-14+4151A>G (HSPA1L) XP_011512868.1:n.-14+4151A>G
NM_005345.6:c.1106T>C (HSPA1A) MANE Select NP_005336.3:p.Val369Ala