Canonical Allele Identifier: CA1619307523
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816429G= , CM000668.2:g.31816429G= GRCh38
NC_000006.11:g.31784206G= , CM000668.1:g.31784206G= GRCh37
NC_000006.10:g.31892185G= NCBI36
NG_011855.1:g.3630C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.673G= (HSPA1A) MANE Select ENSP00000364802.5:p.Asp225=
ENST00000375651.6:c.673G= (HSPA1A) ENSP00000364802.5:p.Asp225=
ENST00000608703.1:c.178G= (HSPA1A) ENSP00000477378.1:p.Asp60=
NM_005345.5:c.673G= (HSPA1A) NP_005336.3:p.Asp225=
XM_005249073.2:c.-13-4444C= (HSPA1L) XP_005249130.1:n.-13-4444C=
XM_011514566.1:c.-13-4444C= (HSPA1L) XP_011512868.1:n.-13-4444C=
NM_005345.6:c.673G= (HSPA1A) MANE Select NP_005336.3:p.Asp225=