Canonical Allele Identifier: CA363413962
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31816745-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816745A>G , CM000668.2:g.31816745A>G GRCh38
NC_000006.11:g.31784522A>G , CM000668.1:g.31784522A>G GRCh37
NC_000006.10:g.31892501A>G NCBI36
NG_011855.1:g.3314T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.989A>G (HSPA1A) MANE Select ENSP00000364802.5:p.Gln330Arg
ENST00000375651.6:c.989A>G (HSPA1A) ENSP00000364802.5:p.Gln330Arg
ENST00000608703.1:c.494A>G (HSPA1A) ENSP00000477378.1:p.Gln165Arg
NM_005345.5:c.989A>G (HSPA1A) NP_005336.3:p.Gln330Arg
XM_005249073.2:c.-14+4268T>C (HSPA1L) XP_005249130.1:n.-14+4268T>C
XM_011514566.1:c.-14+4268T>C (HSPA1L) XP_011512868.1:n.-14+4268T>C
NM_005345.6:c.989A>G (HSPA1A) MANE Select NP_005336.3:p.Gln330Arg