Canonical Allele Identifier: CA3724183
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI
gnomAD v2:
6:31783507 G / C
gnomAD v3:
6:31815730 G / C
gnomAD v4:
chr6-31815730-G-C
Joint Max Group AF 0.73667138 (AFR)
Genomes Max Group AF 0.72865627 (AFR)
Exomes Max Group AF 0.74184465 (AFR)
ClinVar RCV:
RCV000856576
ClinVar Variation:
694516
dbSNP:
1043618
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31815730G>C , CM000668.2:g.31815730G>C GRCh38
NC_000006.11:g.31783507G>C , CM000668.1:g.31783507G>C GRCh37
NC_000006.10:g.31891486G>C NCBI36
NG_011855.1:g.4329C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.-27G>C (HSPA1A) MANE Select ENSP00000364802.5:n.-27G>C
ENST00000375651.6:c.-27G>C (HSPA1A) ENSP00000364802.5:n.-27G>C
ENST00000608703.1:c.-27G>C (HSPA1A) ENSP00000477378.1:n.-27G>C
NM_005345.5:c.-27G>C (HSPA1A) NP_005336.3:n.-27G>C
XM_005249073.2:c.-13-3745C>G (HSPA1L) XP_005249130.1:n.-13-3745C>G
XM_011514566.1:c.-13-3745C>G (HSPA1L) XP_011512868.1:n.-13-3745C>G
NM_005345.6:c.-27G>C (HSPA1A) MANE Select NP_005336.3:n.-27G>C
Search 100 bp 5'
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