Canonical Allele Identifier: CA449806728
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

gnomAD v4: 6-31817292-G-A
MyVariant Identifiers: chr6:g.31785069G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817292G>A , CM000668.2:g.31817292G>A GRCh38
NC_000006.11:g.31785069G>A , CM000668.1:g.31785069G>A GRCh37
NC_000006.10:g.31893048G>A NCBI36
NG_011855.1:g.2767C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1536G>A (HSPA1A) MANE Select ENSP00000364802.5:p.Lys512=
ENST00000375651.6:c.1536G>A (HSPA1A) ENSP00000364802.5:p.Lys512=
ENST00000608703.1:c.1041G>A (HSPA1A) ENSP00000477378.1:p.Lys347=
NM_005345.5:c.1536G>A (HSPA1A) NP_005336.3:p.Lys512=
XM_005249073.2:c.-14+3721C>T (HSPA1L) XP_005249130.1:n.-14+3721C>T
XM_011514566.1:c.-14+3721C>T (HSPA1L) XP_011512868.1:n.-14+3721C>T
NM_005345.6:c.1536G>A (HSPA1A) MANE Select NP_005336.3:p.Lys512=
Search 100 bp 5'
Search 100 bp 3'