Canonical Allele Identifier: CA1619307537
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816809G= , CM000668.2:g.31816809G= GRCh38
NC_000006.11:g.31784586G= , CM000668.1:g.31784586G= GRCh37
NC_000006.10:g.31892565G= NCBI36
NG_011855.1:g.3250C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375651.7:c.1053G= (HSPA1A) MANE Select ENSP00000364802.5:p.Gln351=
ENST00000375651.6:c.1053G= (HSPA1A) ENSP00000364802.5:p.Gln351=
ENST00000608703.1:c.558G= (HSPA1A) ENSP00000477378.1:p.Gln186=
NM_005345.5:c.1053G= (HSPA1A) NP_005336.3:p.Gln351=
XM_005249073.2:c.-14+4204C= (HSPA1L) XP_005249130.1:n.-14+4204C=
XM_011514566.1:c.-14+4204C= (HSPA1L) XP_011512868.1:n.-14+4204C=
NM_005345.6:c.1053G= (HSPA1A) MANE Select NP_005336.3:p.Gln351=