Canonical Allele Identifier: CA1619307607
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817198A= , CM000668.2:g.31817198A= GRCh38
NC_000006.11:g.31784975A= , CM000668.1:g.31784975A= GRCh37
NC_000006.10:g.31892954A= NCBI36
NG_011855.1:g.2861T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1442A= (HSPA1A) MANE Select ENSP00000364802.5:p.Asp481=
ENST00000375651.6:c.1442A= (HSPA1A) ENSP00000364802.5:p.Asp481=
ENST00000608703.1:c.947A= (HSPA1A) ENSP00000477378.1:p.Asp316=
NM_005345.5:c.1442A= (HSPA1A) NP_005336.3:p.Asp481=
XM_005249073.2:c.-14+3815T= (HSPA1L) XP_005249130.1:n.-14+3815T=
XM_011514566.1:c.-14+3815T= (HSPA1L) XP_011512868.1:n.-14+3815T=
NM_005345.6:c.1442A= (HSPA1A) MANE Select NP_005336.3:p.Asp481=
Search 100 bp 5'
Search 100 bp 3'