Canonical Allele Identifier: CA1087483870
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

dbSNP Id: rs1815991412

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817296dup , CM000668.2:g.31817296dup GRCh38
NC_000006.11:g.31785073dup , CM000668.1:g.31785073dup GRCh37
NC_000006.10:g.31893052dup NCBI36
NG_011855.1:g.2764dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1540dup (HSPA1A) MANE Select ENSP00000364802.5:p.Glu514GlyfsTer?
ENST00000375651.6:c.1540dup (HSPA1A) ENSP00000364802.5:p.Glu514GlyfsTer?
ENST00000608703.1:c.1045dup (HSPA1A) ENSP00000477378.1:p.Glu349GlyfsTer?
NM_005345.5:c.1540dup (HSPA1A) NP_005336.3:p.Glu514GlyfsTer?
XM_005249073.2:c.-14+3718dup (HSPA1L) XP_005249130.1:n.-14+3718dup
XM_011514566.1:c.-14+3718dup (HSPA1L) XP_011512868.1:n.-14+3718dup
NM_005345.6:c.1540dup (HSPA1A) MANE Select NP_005336.3:p.Glu514GlyfsTer?