Canonical Allele Identifier: CA363420038
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

dbSNP Id: rs1366756759
MyVariant Identifiers: chr6:g.31785079G>C (hg19) chr6:g.31817302G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817302G>C , CM000668.2:g.31817302G>C GRCh38
NC_000006.11:g.31785079G>C , CM000668.1:g.31785079G>C GRCh37
NC_000006.10:g.31893058G>C NCBI36
NG_011855.1:g.2757C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1546G>C (HSPA1A) MANE Select ENSP00000364802.5:p.Glu516Gln
ENST00000375651.6:c.1546G>C (HSPA1A) ENSP00000364802.5:p.Glu516Gln
ENST00000608703.1:c.1051G>C (HSPA1A) ENSP00000477378.1:p.Glu351Gln
NM_005345.5:c.1546G>C (HSPA1A) NP_005336.3:p.Glu516Gln
XM_005249073.2:c.-14+3711C>G (HSPA1L) XP_005249130.1:n.-14+3711C>G
XM_011514566.1:c.-14+3711C>G (HSPA1L) XP_011512868.1:n.-14+3711C>G
NM_005345.6:c.1546G>C (HSPA1A) MANE Select NP_005336.3:p.Glu516Gln
Search 100 bp 5'
Search 100 bp 3'