Canonical Allele Identifier: CA1619307602
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817191G= , CM000668.2:g.31817191G= GRCh38
NC_000006.11:g.31784968G= , CM000668.1:g.31784968G= GRCh37
NC_000006.10:g.31892947G= NCBI36
NG_011855.1:g.2868C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1435G= (HSPA1A) MANE Select ENSP00000364802.5:p.Asp479=
ENST00000375651.6:c.1435G= (HSPA1A) ENSP00000364802.5:p.Asp479=
ENST00000608703.1:c.940G= (HSPA1A) ENSP00000477378.1:p.Asp314=
NM_005345.5:c.1435G= (HSPA1A) NP_005336.3:p.Asp479=
XM_005249073.2:c.-14+3822C= (HSPA1L) XP_005249130.1:n.-14+3822C=
XM_011514566.1:c.-14+3822C= (HSPA1L) XP_011512868.1:n.-14+3822C=
NM_005345.6:c.1435G= (HSPA1A) MANE Select NP_005336.3:p.Asp479=
Search 100 bp 5'
Search 100 bp 3'