Canonical Allele Identifier: CA1619307620

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817231A= , CM000668.2:g.31817231A=	GRCh38
NC_000006.11:g.31785008A= , CM000668.1:g.31785008A=	GRCh37
NC_000006.10:g.31892987A=	NCBI36
NG_011855.1:g.2828T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1475A= (HSPA1A) MANE Select	ENSP00000364802.5:p.Asp492=
ENST00000375651.6:c.1475A= (HSPA1A)	ENSP00000364802.5:p.Asp492=
ENST00000608703.1:c.980A= (HSPA1A)	ENSP00000477378.1:p.Asp327=
NM_005345.5:c.1475A= (HSPA1A)	NP_005336.3:p.Asp492=
XM_005249073.2:c.-14+3782T= (HSPA1L)	XP_005249130.1:n.-14+3782T=
XM_011514566.1:c.-14+3782T= (HSPA1L)	XP_011512868.1:n.-14+3782T=
NM_005345.6:c.1475A= (HSPA1A) MANE Select	NP_005336.3:p.Asp492=