Canonical Allele Identifier: CA449806131

Gene: HSPA1A HSPA1L

Linked Data

• MyVariant Identifiers: chr6:g.31784314A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816537A>C , CM000668.2:g.31816537A>C	GRCh38
NC_000006.11:g.31784314A>C , CM000668.1:g.31784314A>C	GRCh37
NC_000006.10:g.31892293A>C	NCBI36
NG_011855.1:g.3522T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.781A>C (HSPA1A) MANE Select	ENSP00000364802.5:p.Arg261=
ENST00000375651.6:c.781A>C (HSPA1A)	ENSP00000364802.5:p.Arg261=
ENST00000608703.1:c.286A>C (HSPA1A)	ENSP00000477378.1:p.Arg96=
NM_005345.5:c.781A>C (HSPA1A)	NP_005336.3:p.Arg261=
XM_005249073.2:c.-14+4476T>G (HSPA1L)	XP_005249130.1:n.-14+4476T>G
XM_011514566.1:c.-14+4476T>G (HSPA1L)	XP_011512868.1:n.-14+4476T>G
NM_005345.6:c.781A>C (HSPA1A) MANE Select	NP_005336.3:p.Arg261=