Canonical Allele Identifier: CA1619307618

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817228C= , CM000668.2:g.31817228C=	GRCh38
NC_000006.11:g.31785005C= , CM000668.1:g.31785005C=	GRCh37
NC_000006.10:g.31892984C=	NCBI36
NG_011855.1:g.2831G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1472C= (HSPA1A) MANE Select	ENSP00000364802.5:p.Thr491=
ENST00000375651.6:c.1472C= (HSPA1A)	ENSP00000364802.5:p.Thr491=
ENST00000608703.1:c.977C= (HSPA1A)	ENSP00000477378.1:p.Thr326=
NM_005345.5:c.1472C= (HSPA1A)	NP_005336.3:p.Thr491=
XM_005249073.2:c.-14+3785G= (HSPA1L)	XP_005249130.1:n.-14+3785G=
XM_011514566.1:c.-14+3785G= (HSPA1L)	XP_011512868.1:n.-14+3785G=
NM_005345.6:c.1472C= (HSPA1A) MANE Select	NP_005336.3:p.Thr491=