Canonical Allele Identifier: CA449805829
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31816425-C-A
MyVariant Identifiers: chr6:g.31784202C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816425C>A , CM000668.2:g.31816425C>A GRCh38
NC_000006.11:g.31784202C>A , CM000668.1:g.31784202C>A GRCh37
NC_000006.10:g.31892181C>A NCBI36
NG_011855.1:g.3634G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.669C>A (HSPA1A) MANE Select ENSP00000364802.5:p.Ala223=
ENST00000375651.6:c.669C>A (HSPA1A) ENSP00000364802.5:p.Ala223=
ENST00000608703.1:c.174C>A (HSPA1A) ENSP00000477378.1:p.Ala58=
NM_005345.5:c.669C>A (HSPA1A) NP_005336.3:p.Ala223=
XM_005249073.2:c.-13-4440G>T (HSPA1L) XP_005249130.1:n.-13-4440G>T
XM_011514566.1:c.-13-4440G>T (HSPA1L) XP_011512868.1:n.-13-4440G>T
NM_005345.6:c.669C>A (HSPA1A) MANE Select NP_005336.3:p.Ala223=
Search 100 bp 5'
Search 100 bp 3'