Canonical Allele Identifier: CA2678043528
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816501_31816505del , CM000668.2:g.31816501_31816505del GRCh38
NC_000006.11:g.31784278_31784282del , CM000668.1:g.31784278_31784282del GRCh37
NC_000006.10:g.31892257_31892261del NCBI36
NG_011855.1:g.3556_3560del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.745_749del (HSPA1A) MANE Select ENSP00000364802.5:p.His249GlufsTer?
ENST00000375651.6:c.745_749del (HSPA1A) ENSP00000364802.5:p.His249GlufsTer?
ENST00000608703.1:c.250_254del (HSPA1A) ENSP00000477378.1:p.His84GlufsTer?
NM_005345.5:c.745_749del (HSPA1A) NP_005336.3:p.His249GlufsTer?
XM_005249073.2:c.-14+4510_-13-4514del (HSPA1L) XP_005249130.1:n.-14+4510_-13-4514del
XM_011514566.1:c.-14+4510_-13-4514del (HSPA1L) XP_011512868.1:n.-14+4510_-13-4514del
NM_005345.6:c.745_749del (HSPA1A) MANE Select NP_005336.3:p.His249GlufsTer?