Canonical Allele Identifier: CA1619307581
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817113A= , CM000668.2:g.31817113A= GRCh38
NC_000006.11:g.31784890A= , CM000668.1:g.31784890A= GRCh37
NC_000006.10:g.31892869A= NCBI36
NG_011855.1:g.2946T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1357A= (HSPA1A) MANE Select ENSP00000364802.5:p.Asn453=
ENST00000375651.6:c.1357A= (HSPA1A) ENSP00000364802.5:p.Asn453=
ENST00000608703.1:c.862A= (HSPA1A) ENSP00000477378.1:p.Asn288=
NM_005345.5:c.1357A= (HSPA1A) NP_005336.3:p.Asn453=
XM_005249073.2:c.-14+3900T= (HSPA1L) XP_005249130.1:n.-14+3900T=
XM_011514566.1:c.-14+3900T= (HSPA1L) XP_011512868.1:n.-14+3900T=
NM_005345.6:c.1357A= (HSPA1A) MANE Select NP_005336.3:p.Asn453=
Search 100 bp 5'
Search 100 bp 3'