Canonical Allele Identifier: CA363418841
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

dbSNP Id: rs1327237373
gnomAD v2: 6-31784993-A-G
gnomAD v4: 6-31817216-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817216A>G , CM000668.2:g.31817216A>G GRCh38
NC_000006.11:g.31784993A>G , CM000668.1:g.31784993A>G GRCh37
NC_000006.10:g.31892972A>G NCBI36
NG_011855.1:g.2843T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1460A>G (HSPA1A) MANE Select ENSP00000364802.5:p.Asn487Ser
ENST00000375651.6:c.1460A>G (HSPA1A) ENSP00000364802.5:p.Asn487Ser
ENST00000608703.1:c.965A>G (HSPA1A) ENSP00000477378.1:p.Asn322Ser
NM_005345.5:c.1460A>G (HSPA1A) NP_005336.3:p.Asn487Ser
XM_005249073.2:c.-14+3797T>C (HSPA1L) XP_005249130.1:n.-14+3797T>C
XM_011514566.1:c.-14+3797T>C (HSPA1L) XP_011512868.1:n.-14+3797T>C
NM_005345.6:c.1460A>G (HSPA1A) MANE Select NP_005336.3:p.Asn487Ser