Canonical Allele Identifier: CA363412597
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31816642-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816642T>A , CM000668.2:g.31816642T>A GRCh38
NC_000006.11:g.31784419T>A , CM000668.1:g.31784419T>A GRCh37
NC_000006.10:g.31892398T>A NCBI36
NG_011855.1:g.3417A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.886T>A (HSPA1A) MANE Select ENSP00000364802.5:p.Ser296Thr
ENST00000375651.6:c.886T>A (HSPA1A) ENSP00000364802.5:p.Ser296Thr
ENST00000608703.1:c.391T>A (HSPA1A) ENSP00000477378.1:p.Ser131Thr
NM_005345.5:c.886T>A (HSPA1A) NP_005336.3:p.Ser296Thr
XM_005249073.2:c.-14+4371A>T (HSPA1L) XP_005249130.1:n.-14+4371A>T
XM_011514566.1:c.-14+4371A>T (HSPA1L) XP_011512868.1:n.-14+4371A>T
NM_005345.6:c.886T>A (HSPA1A) MANE Select NP_005336.3:p.Ser296Thr