Canonical Allele Identifier: CA363410604
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816481T>C , CM000668.2:g.31816481T>C GRCh38
NC_000006.11:g.31784258T>C , CM000668.1:g.31784258T>C GRCh37
NC_000006.10:g.31892237T>C NCBI36
NG_011855.1:g.3578A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.725T>C (HSPA1A) MANE Select ENSP00000364802.5:p.Val242Ala
ENST00000375651.6:c.725T>C (HSPA1A) ENSP00000364802.5:p.Val242Ala
ENST00000608703.1:c.230T>C (HSPA1A) ENSP00000477378.1:p.Val77Ala
NM_005345.5:c.725T>C (HSPA1A) NP_005336.3:p.Val242Ala
XM_005249073.2:c.-13-4496A>G (HSPA1L) XP_005249130.1:n.-13-4496A>G
XM_011514566.1:c.-13-4496A>G (HSPA1L) XP_011512868.1:n.-13-4496A>G
NM_005345.6:c.725T>C (HSPA1A) MANE Select NP_005336.3:p.Val242Ala