Canonical Allele Identifier: CA363419562
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31817272-G-T
MyVariant Identifiers: chr6:g.31785049G>T (hg19) chr6:g.31817272G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817272G>T , CM000668.2:g.31817272G>T GRCh38
NC_000006.11:g.31785049G>T , CM000668.1:g.31785049G>T GRCh37
NC_000006.10:g.31893028G>T NCBI36
NG_011855.1:g.2787C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1516G>T (HSPA1A) MANE Select ENSP00000364802.5:p.Asp506Tyr
ENST00000375651.6:c.1516G>T (HSPA1A) ENSP00000364802.5:p.Asp506Tyr
ENST00000608703.1:c.1021G>T (HSPA1A) ENSP00000477378.1:p.Asp341Tyr
NM_005345.5:c.1516G>T (HSPA1A) NP_005336.3:p.Asp506Tyr
XM_005249073.2:c.-14+3741C>A (HSPA1L) XP_005249130.1:n.-14+3741C>A
XM_011514566.1:c.-14+3741C>A (HSPA1L) XP_011512868.1:n.-14+3741C>A
NM_005345.6:c.1516G>T (HSPA1A) MANE Select NP_005336.3:p.Asp506Tyr
Search 100 bp 5'
Search 100 bp 3'