Canonical Allele Identifier: CA363419898
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817295G>T , CM000668.2:g.31817295G>T GRCh38
NC_000006.11:g.31785072G>T , CM000668.1:g.31785072G>T GRCh37
NC_000006.10:g.31893051G>T NCBI36
NG_011855.1:g.2764C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1539G>T (HSPA1A) MANE Select ENSP00000364802.5:p.Glu513Asp
ENST00000375651.6:c.1539G>T (HSPA1A) ENSP00000364802.5:p.Glu513Asp
ENST00000608703.1:c.1044G>T (HSPA1A) ENSP00000477378.1:p.Glu348Asp
NM_005345.5:c.1539G>T (HSPA1A) NP_005336.3:p.Glu513Asp
XM_005249073.2:c.-14+3718C>A (HSPA1L) XP_005249130.1:n.-14+3718C>A
XM_011514566.1:c.-14+3718C>A (HSPA1L) XP_011512868.1:n.-14+3718C>A
NM_005345.6:c.1539G>T (HSPA1A) MANE Select NP_005336.3:p.Glu513Asp