Canonical Allele Identifier: CA1619307619

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817229G= , CM000668.2:g.31817229G=	GRCh38
NC_000006.11:g.31785006G= , CM000668.1:g.31785006G=	GRCh37
NC_000006.10:g.31892985G=	NCBI36
NG_011855.1:g.2830C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1473G= (HSPA1A) MANE Select	ENSP00000364802.5:p.Thr491=
ENST00000375651.6:c.1473G= (HSPA1A)	ENSP00000364802.5:p.Thr491=
ENST00000608703.1:c.978G= (HSPA1A)	ENSP00000477378.1:p.Thr326=
NM_005345.5:c.1473G= (HSPA1A)	NP_005336.3:p.Thr491=
XM_005249073.2:c.-14+3784C= (HSPA1L)	XP_005249130.1:n.-14+3784C=
XM_011514566.1:c.-14+3784C= (HSPA1L)	XP_011512868.1:n.-14+3784C=
NM_005345.6:c.1473G= (HSPA1A) MANE Select	NP_005336.3:p.Thr491=