Canonical Allele Identifier: CA449805925
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31784556C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816779C>A , CM000668.2:g.31816779C>A GRCh38
NC_000006.11:g.31784556C>A , CM000668.1:g.31784556C>A GRCh37
NC_000006.10:g.31892535C>A NCBI36
NG_011855.1:g.3280G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1023C>A (HSPA1A) MANE Select ENSP00000364802.5:p.Thr341=
ENST00000375651.6:c.1023C>A (HSPA1A) ENSP00000364802.5:p.Thr341=
ENST00000608703.1:c.528C>A (HSPA1A) ENSP00000477378.1:p.Thr176=
NM_005345.5:c.1023C>A (HSPA1A) NP_005336.3:p.Thr341=
XM_005249073.2:c.-14+4234G>T (HSPA1L) XP_005249130.1:n.-14+4234G>T
XM_011514566.1:c.-14+4234G>T (HSPA1L) XP_011512868.1:n.-14+4234G>T
NM_005345.6:c.1023C>A (HSPA1A) MANE Select NP_005336.3:p.Thr341=
Search 100 bp 5'
Search 100 bp 3'