Canonical Allele Identifier: CA363410230
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31816453-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816453T>G , CM000668.2:g.31816453T>G GRCh38
NC_000006.11:g.31784230T>G , CM000668.1:g.31784230T>G GRCh37
NC_000006.10:g.31892209T>G NCBI36
NG_011855.1:g.3606A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.697T>G (HSPA1A) MANE Select ENSP00000364802.5:p.Phe233Val
ENST00000375651.6:c.697T>G (HSPA1A) ENSP00000364802.5:p.Phe233Val
ENST00000608703.1:c.202T>G (HSPA1A) ENSP00000477378.1:p.Phe68Val
NM_005345.5:c.697T>G (HSPA1A) NP_005336.3:p.Phe233Val
XM_005249073.2:c.-13-4468A>C (HSPA1L) XP_005249130.1:n.-13-4468A>C
XM_011514566.1:c.-13-4468A>C (HSPA1L) XP_011512868.1:n.-13-4468A>C
NM_005345.6:c.697T>G (HSPA1A) MANE Select NP_005336.3:p.Phe233Val