Canonical Allele Identifier: CA363413635
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816714G>A , CM000668.2:g.31816714G>A GRCh38
NC_000006.11:g.31784491G>A , CM000668.1:g.31784491G>A GRCh37
NC_000006.10:g.31892470G>A NCBI36
NG_011855.1:g.3345C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375651.7:c.958G>A (HSPA1A) MANE Select ENSP00000364802.5:p.Ala320Thr
ENST00000375651.6:c.958G>A (HSPA1A) ENSP00000364802.5:p.Ala320Thr
ENST00000608703.1:c.463G>A (HSPA1A) ENSP00000477378.1:p.Ala155Thr
NM_005345.5:c.958G>A (HSPA1A) NP_005336.3:p.Ala320Thr
XM_005249073.2:c.-14+4299C>T (HSPA1L) XP_005249130.1:n.-14+4299C>T
XM_011514566.1:c.-14+4299C>T (HSPA1L) XP_011512868.1:n.-14+4299C>T
NM_005345.6:c.958G>A (HSPA1A) MANE Select NP_005336.3:p.Ala320Thr