Canonical Allele Identifier: CA1619307643

Gene: HSPA1A HSPA1L

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31817284C= , CM000668.2:g.31817284C=	GRCh38
NC_000006.11:g.31785061C= , CM000668.1:g.31785061C=	GRCh37
NC_000006.10:g.31893040C=	NCBI36
NG_011855.1:g.2775G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1528C= (HSPA1A) MANE Select	ENSP00000364802.5:p.Leu510=
ENST00000375651.6:c.1528C= (HSPA1A)	ENSP00000364802.5:p.Leu510=
ENST00000608703.1:c.1033C= (HSPA1A)	ENSP00000477378.1:p.Leu345=
NM_005345.5:c.1528C= (HSPA1A)	NP_005336.3:p.Leu510=
XM_005249073.2:c.-14+3729G= (HSPA1L)	XP_005249130.1:n.-14+3729G=
XM_011514566.1:c.-14+3729G= (HSPA1L)	XP_011512868.1:n.-14+3729G=
NM_005345.6:c.1528C= (HSPA1A) MANE Select	NP_005336.3:p.Leu510=