Canonical Allele Identifier: CA363419372
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31785036C>G (hg19) chr6:g.31817259C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817259C>G , CM000668.2:g.31817259C>G GRCh38
NC_000006.11:g.31785036C>G , CM000668.1:g.31785036C>G GRCh37
NC_000006.10:g.31893015C>G NCBI36
NG_011855.1:g.2800G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1503C>G (HSPA1A) MANE Select ENSP00000364802.5:p.Ile501Met
ENST00000375651.6:c.1503C>G (HSPA1A) ENSP00000364802.5:p.Ile501Met
ENST00000608703.1:c.1008C>G (HSPA1A) ENSP00000477378.1:p.Ile336Met
NM_005345.5:c.1503C>G (HSPA1A) NP_005336.3:p.Ile501Met
XM_005249073.2:c.-14+3754G>C (HSPA1L) XP_005249130.1:n.-14+3754G>C
XM_011514566.1:c.-14+3754G>C (HSPA1L) XP_011512868.1:n.-14+3754G>C
NM_005345.6:c.1503C>G (HSPA1A) MANE Select NP_005336.3:p.Ile501Met
Search 100 bp 5'
Search 100 bp 3'