Canonical Allele Identifier: CA363419100
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817237G>C , CM000668.2:g.31817237G>C GRCh38
NC_000006.11:g.31785014G>C , CM000668.1:g.31785014G>C GRCh37
NC_000006.10:g.31892993G>C NCBI36
NG_011855.1:g.2822C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1481G>C (HSPA1A) MANE Select ENSP00000364802.5:p.Ser494Thr
ENST00000375651.6:c.1481G>C (HSPA1A) ENSP00000364802.5:p.Ser494Thr
ENST00000608703.1:c.986G>C (HSPA1A) ENSP00000477378.1:p.Ser329Thr
NM_005345.5:c.1481G>C (HSPA1A) NP_005336.3:p.Ser494Thr
XM_005249073.2:c.-14+3776C>G (HSPA1L) XP_005249130.1:n.-14+3776C>G
XM_011514566.1:c.-14+3776C>G (HSPA1L) XP_011512868.1:n.-14+3776C>G
NM_005345.6:c.1481G>C (HSPA1A) MANE Select NP_005336.3:p.Ser494Thr