Canonical Allele Identifier: CA363418679

Gene: HSPA1A HSPA1L

Linked Data

• MyVariant Identifiers: chr6:g.31784983G>C (hg19) ; chr6:g.31817206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817206G>C , CM000668.2:g.31817206G>C	GRCh38
NC_000006.11:g.31784983G>C , CM000668.1:g.31784983G>C	GRCh37
NC_000006.10:g.31892962G>C	NCBI36
NG_011855.1:g.2853C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1450G>C (HSPA1A) MANE Select	ENSP00000364802.5:p.Gly484Arg
ENST00000375651.6:c.1450G>C (HSPA1A)	ENSP00000364802.5:p.Gly484Arg
ENST00000608703.1:c.955G>C (HSPA1A)	ENSP00000477378.1:p.Gly319Arg
NM_005345.5:c.1450G>C (HSPA1A)	NP_005336.3:p.Gly484Arg
XM_005249073.2:c.-14+3807C>G (HSPA1L)	XP_005249130.1:n.-14+3807C>G
XM_011514566.1:c.-14+3807C>G (HSPA1L)	XP_011512868.1:n.-14+3807C>G
NM_005345.6:c.1450G>C (HSPA1A) MANE Select	NP_005336.3:p.Gly484Arg