Canonical Allele Identifier: CA363412560
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816636T>G , CM000668.2:g.31816636T>G GRCh38
NC_000006.11:g.31784413T>G , CM000668.1:g.31784413T>G GRCh37
NC_000006.10:g.31892392T>G NCBI36
NG_011855.1:g.3423A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.880T>G (HSPA1A) MANE Select ENSP00000364802.5:p.Tyr294Asp
ENST00000375651.6:c.880T>G (HSPA1A) ENSP00000364802.5:p.Tyr294Asp
ENST00000608703.1:c.385T>G (HSPA1A) ENSP00000477378.1:p.Tyr129Asp
NM_005345.5:c.880T>G (HSPA1A) NP_005336.3:p.Tyr294Asp
XM_005249073.2:c.-14+4377A>C (HSPA1L) XP_005249130.1:n.-14+4377A>C
XM_011514566.1:c.-14+4377A>C (HSPA1L) XP_011512868.1:n.-14+4377A>C
NM_005345.6:c.880T>G (HSPA1A) MANE Select NP_005336.3:p.Tyr294Asp