Canonical Allele Identifier: CA363410403
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31816469-T-A
MyVariant Identifiers: chr6:g.31784246T>A (hg19) chr6:g.31816469T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816469T>A , CM000668.2:g.31816469T>A GRCh38
NC_000006.11:g.31784246T>A , CM000668.1:g.31784246T>A GRCh37
NC_000006.10:g.31892225T>A NCBI36
NG_011855.1:g.3590A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.713T>A (HSPA1A) MANE Select ENSP00000364802.5:p.Val238Glu
ENST00000375651.6:c.713T>A (HSPA1A) ENSP00000364802.5:p.Val238Glu
ENST00000608703.1:c.218T>A (HSPA1A) ENSP00000477378.1:p.Val73Glu
NM_005345.5:c.713T>A (HSPA1A) NP_005336.3:p.Val238Glu
XM_005249073.2:c.-13-4484A>T (HSPA1L) XP_005249130.1:n.-13-4484A>T
XM_011514566.1:c.-13-4484A>T (HSPA1L) XP_011512868.1:n.-13-4484A>T
NM_005345.6:c.713T>A (HSPA1A) MANE Select NP_005336.3:p.Val238Glu
Search 100 bp 5'
Search 100 bp 3'