Canonical Allele Identifier: CA363417392
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31817087-A-T
MyVariant Identifiers: chr6:g.31784864A>T (hg19) chr6:g.31817087A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817087A>T , CM000668.2:g.31817087A>T GRCh38
NC_000006.11:g.31784864A>T , CM000668.1:g.31784864A>T GRCh37
NC_000006.10:g.31892843A>T NCBI36
NG_011855.1:g.2972T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1331A>T (HSPA1A) MANE Select ENSP00000364802.5:p.Glu444Val
ENST00000375651.6:c.1331A>T (HSPA1A) ENSP00000364802.5:p.Glu444Val
ENST00000608703.1:c.836A>T (HSPA1A) ENSP00000477378.1:p.Glu279Val
NM_005345.5:c.1331A>T (HSPA1A) NP_005336.3:p.Glu444Val
XM_005249073.2:c.-14+3926T>A (HSPA1L) XP_005249130.1:n.-14+3926T>A
XM_011514566.1:c.-14+3926T>A (HSPA1L) XP_011512868.1:n.-14+3926T>A
NM_005345.6:c.1331A>T (HSPA1A) MANE Select NP_005336.3:p.Glu444Val
Search 100 bp 5'
Search 100 bp 3'